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Sperm Select System,Spermokinesemeters Suppliers & Manufacturers

351 to 400 of 443 results  Page: << Previous 50 Results 1 2 3 4 5 6 7 [8] 9 >> Next 50 Results
Sperm Select System
Select Medical Systems, Inc.

Spermokinesemeters
Gamogen, Inc.

Standard Circumcision Tray (FDA Code: OHG / 884.453)

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

Southpointe Surgical Supply, Inc., Medline Industries, Inc., PST Corporation, more...

Standard Hysteroscopic Equipment
Cook Urological

Sterile Umbilical Tapes
Elantec Medical, Inc., Covidien, Ethicon, Inc., more...

Straight Cervix Holding Forceps
U.S.E Surgical Instruments

Straight Uterine Curette w/Regular Tip
Cooper Surgical, Inc., Marina Medical Instruments Inc., Milex Products, Inc., more...

Straight Uterine Scissors
Waqas Surgical Instruments, Wet Metal

Suction Vacuum Extractor
A suction vacuum extractor is an instrument to assist the delivery of babies. A hand-held pump produces low vacuum, which is applied to a suction cup attached to the exposed fetal head. Traction is applied to the fetal head to assist each contraction. The current trend for instrument-assisted delivery is toward less and less use of forceps. It is a cup like device that is either attached to a suction device on the wall or by a manual suction pump. It is placed on the back of the baby's head and the suction is increased so that the practitioner pulls with the mother's pushes.
Wincup, Toitsu

Surgical microscope for Gynecologist Surgeons
Carl Zeiss Meditec, Inc., Marco, Techman International Corporation, more...

Synthetic Condom (FDA Code: MOL / 884.53)

Identification. A condom is a sheath which completely covers the penis with a closely fitting membrane. The condom is used for contraceptive and for prophylactic purposes (preventing transmission of venereal disease). The device may also be used to collect semen to aid in the diagnosis of infertility.

Classification. Class II (performance standards).

Mayer Laboratories, Inc., Instead Healthcare, Inc., Adelphia Discount Services Inc., more...

Synthetic Osmotic Cervical Dilator (FDA Code: LOB)
Medtronic Xomed Surgical Products, Inc, Gelmed International

Tenaculm Forceps
Sklar Instruments

Tenaculum Hooks
Sklar Instruments

Tenaculums
Tenaculums is an instrument consisting of a fine, sharp hook attached to a handle and used mainly for taking up arteries.
Sklar Instruments, Miltex, Inc., Premier Medical Products, more...

Therapeutic Vaginal Douche Apparatus (FDA Code: HED / 884.59)

Identification. A therapeutic vaginal douche apparatus is a device that is a bag or bottle with tubing and a nozzle. The apparatus does not include douche solutions. The apparatus is intended and labeled for use in the treatment of medical conditions except it is not for contraceptive use. After filling the therapeutic vaginal douche apparatus with a solution, the patient uses the device to direct a stream of solution into the vaginal cavity.

Classification. (1) Class II (performance standards).

Autosuture, Hospira, Inc., Techworld Medicals, Inc., more...

Tightening Umbilical Tapes
Elantec Medical, Inc., Covidien, Ethicon, Inc., more...

Tissue Forceps
Medical Supply Group, Dealmed Medical Supplies, Sklar Instruments, more...

Traction Forceps
Sklar Instruments

Transabdominal Amnioscope and Accessories (FDA Code: HFA / 884.16)

Identification. A transabdominal amnioscope is a device designed to permit direct visual examination of the fetus by a telescopic system via abdominal entry. The device is used to ascertain fetal abnormalities, to obtain fetal blood samples, or to obtain fetal tissue. This generic type of device may include the following accessories: trocar and cannula, instruments used through an operating channel or through a separate cannula associated with the amnioscope, light source and cables, and component parts.

Classification. Class III (premarket approval).

Allen Medical Instruments Corp., Guidant Corporation, Karl Storz GmbH & Co. KG.

Transcervical Balloon Catheter (FDA Code: MKN)
Ethicon, Inc., Conceptus, Inc., Hei Inc., Advanced Medical Division, more...

Transcervical Endoscope & Accessories (FDA Code: HEZ / 884.166)

Identification. A transcervical endoscope is a device designed to permit direct viewing of the fetus and amniotic sac by means of an open tube introduced into the uterus through the cervix. The device may be used to visualize the fetus or amniotic fluid and to sample fetal blood or amniotic fluid. This generic type of device may include obturators, instruments used through an operating channel, light sources and cables, and component parts.

Classification. Class II (performance standards).

Treier Endoscopie AG, Richard Wolf GmbH, Karl Storz GmbH & Co. KG.

Tubal Ligation Kits
Safestitch Medical, Abnova Taiwan Corporation, Thd Spa, more...

Tubal Occlusion Band (FDA Code: HFY / 884.538)

Identification. A contraceptive tubal occlusion device (TOD) and introducer is a device designed to close a fallopian tube with a mechanical structure, e.g., a band or clip on the outside of the fallopian tube or a plug or valve on the inside. The devices are used to prevent pregnancy.

Classification. Class III (premarket approval).

Aleph One Limited

Tubal Occlusion Insert (FDA Code: HHS / 884.538)

Identification. A contraceptive tubal occlusion device (TOD) and introducer is a device designed to close a fallopian tube with a mechanical structure, e.g., a band or clip on the outside of the fallopian tube or a plug or valve on the inside. The devices are used to prevent pregnancy.

Classification. Class III (premarket approval).

Conceptus, Inc., Accellent Inc., Avail Medical Products, Inc., more...

Tubing And Tubing/Filter Fits (FDA Code: NVT / 884.17)

Identification. A hysteroscopic insufflator is a device designed to distend the uterus by filling the uterine cavity with a liquid or gas to facilitate viewing with a hysteroscope.

Classification. (1) Class II (performance standards).

Fujinon, Inc., Rocket Medical, Karl Storz GmbH & Co. KG., more...

Twin Electronic Breast Pump
Twin electronic breast pump is a safe and effective powered breast pump for expressing and collecting breast milk from the breasts of a lactating woman. The pumping can be performed on one breast or two breasts simultaneously, from independent diaphragms. It operates in two modes. In the manual mode, the user controls the frequency and level of vacuum by varying the stroke/cycle of the control handle lever. In the automatic mode, the pumping cycle is stored and controlled by the microprocessor.
Philips Avent

Ultrasonic Blood Flow Monitor (FDA Code: HEP / 884.266)

Identification. A fetal ultrasonic monitor is a device designed to transmit and receive ultrasonic energy into and from the pregnant woman, usually by means of continuous wave (doppler) echoscopy. The device is used to represent some physiological condition or characteristic in a measured value over a period of time (e.g., perinatal monitoring during labor) or in an immediately perceptible form (e.g., use of the ultrasonic stethoscope). This generic type of device may include the following accessories: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, and component parts. This generic type of device does not include devices used to image some relatively unchanging physiological structure or interpret a physiological condition, but does include devices which may be set to alarm automatically at a predetermined threshold value.

Classification. Class II (performance standards).

Vyaire Medical, Inc., Koven Technology, Inc., Medical Equipment Direct, Inc., more...

Ultrasonic Fetal Arterial Pressure Monitor (FDA Code: HEQ / 884.266)

Identification. A fetal ultrasonic monitor is a device designed to transmit and receive ultrasonic energy into and from the pregnant woman, usually by means of continuous wave (doppler) echoscopy. The device is used to represent some physiological condition or characteristic in a measured value over a period of time (e.g., perinatal monitoring during labor) or in an immediately perceptible form (e.g., use of the ultrasonic stethoscope). This generic type of device may include the following accessories: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, and component parts. This generic type of device does not include devices used to image some relatively unchanging physiological structure or interpret a physiological condition, but does include devices which may be set to alarm automatically at a predetermined threshold value.

Classification. Class II (performance standards).

Elmed Inc.

Ultrasonic Fetal Heart Rate Monitor (FDA Code: HEL / 884.266)

Identification. A fetal ultrasonic monitor is a device designed to transmit and receive ultrasonic energy into and from the pregnant woman, usually by means of continuous wave (doppler) echoscopy. The device is used to represent some physiological condition or characteristic in a measured value over a period of time (e.g., perinatal monitoring during labor) or in an immediately perceptible form (e.g., use of the ultrasonic stethoscope). This generic type of device may include the following accessories: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, and component parts. This generic type of device does not include devices used to image some relatively unchanging physiological structure or interpret a physiological condition, but does include devices which may be set to alarm automatically at a predetermined threshold value.

Classification. Class II (performance standards).

Nation Medical Supplies, Polar Electro Inc., Invivo, more...

Ultrasonic Fetal Heart Sound Monitor (FDA Code: HEK / 884.266)

Identification. A fetal ultrasonic monitor is a device designed to transmit and receive ultrasonic energy into and from the pregnant woman, usually by means of continuous wave (doppler) echoscopy. The device is used to represent some physiological condition or characteristic in a measured value over a period of time (e.g., perinatal monitoring during labor) or in an immediately perceptible form (e.g., use of the ultrasonic stethoscope). This generic type of device may include the following accessories: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, and component parts. This generic type of device does not include devices used to image some relatively unchanging physiological structure or interpret a physiological condition, but does include devices which may be set to alarm automatically at a predetermined threshold value.

Classification. Class II (performance standards).

Summit Doppler Systems, Inc., Analogic Corporation, Parks Medical Electronics, Inc., more...

Ultrasonic Fetal Monitor (FDA Code: KNG / 884.266)

Identification. A fetal ultrasonic monitor is a device designed to transmit and receive ultrasonic energy into and from the pregnant woman, usually by means of continuous wave (doppler) echoscopy. The device is used to represent some physiological condition or characteristic in a measured value over a period of time (e.g., perinatal monitoring during labor) or in an immediately perceptible form (e.g., use of the ultrasonic stethoscope). This generic type of device may include the following accessories: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, and component parts. This generic type of device does not include devices used to image some relatively unchanging physiological structure or interpret a physiological condition, but does include devices which may be set to alarm automatically at a predetermined threshold value.

Classification. Class II (performance standards).

Bristol Med Wholesale, Cooper Surgical, Inc., Stork Radio, more...

Ultrasonic Intracorporeal Device Locator (FDA Code: HHJ / 884.2225)

Identification. An obstetric-gynecologic ultrasonic imager is a device designed to transmit and receive ultrasonic energy into and from a female patient by pulsed echoscopy. This device is used to provide a visual representation of some physiological or artificial structure, or of a fetus, for diagnostic purposes during a limited period of time. This generic type of device may include the following: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, coupling gel, and component parts. This generic type of device does not include devices used to monitor the changes in some physiological condition over long periods of time.

Classification. Class II (performance standards).

Medispec Ltd. - USA, Ultraguide Ltd.

Ultrasonic Obstetric-Gynecologic Imager (FDA Code: HEM / 884.2225)

Identification. An obstetric-gynecologic ultrasonic imager is a device designed to transmit and receive ultrasonic energy into and from a female patient by pulsed echoscopy. This device is used to provide a visual representation of some physiological or artificial structure, or of a fetus, for diagnostic purposes during a limited period of time. This generic type of device may include the following: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, coupling gel, and component parts. This generic type of device does not include devices used to monitor the changes in some physiological condition over long periods of time.

Classification. Class II (performance standards).

Siemens Medical Solutions USA Inc, Philips Medical Systems, N.A., Solomon Technology Labs, more...

Umbilical Clamp (FDA Code: HFW / 884.453)

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

Hollister Incorporated, Vyaire Medical, Inc., Teleflex Medical, more...

Umbilical Clamp And Cutter (FDA Code: NBZ / 884.453)

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

Luxtec, Deroyal Surgical - Rose Hill, Pollak International Ltd. Euroband

Umbilical Cord Clamps
Umbilical cord clamp is suitable for clamping the umbilical cord of newly born baby immediately after the birth. It is provided with finger grip for safe and convenient handling. It has a security lock to prevent accidental opening after clamping. It has a grooved clamping area to prevent slipping of the umbilical cord.
CVM Trading Solutions, Online Medical Supply, Aspen Surgical Products, more...

Umbilical Scissors (FDA Code: HDJ / 884.452)

Identification. An obstetric-gynecologic general manual instrument is one of a group of devices used to perform simple obstetric and gynecologic manipulative functions. This generic type of device consists of the following:

Classification. Class I (general controls). The devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 884.9.

KLS Martin, L.P., Vyaire Medical, Inc., Luxtec, more...

Umbilical Tapes
Syneture, Ethicon, Inc., CP Medical, Inc, more...

Unipolar Endoscopic Coagulator-cutter and Accessories (FDA Code: KNF / 884.416)

Identification. A unipolar endoscopic coagulator-cutter is a device designed to destroy tissue with high temperatures by directing a high frequency electrical current through the tissue between an energized probe and a grounding plate. It is used in female sterilization and in other operative procedures under endoscopic observation. This generic type of device may include the following accessories: an electrical generator, probes and electrical cables, and a patient grounding plate. This generic type of device does not include devices used to perform female sterilization under hysteroscopic observation.

Classification. Class II (performance standards).

TTI Medical, Advanced Bionics Corporation, Bovie Medical Corporation, more...

Unipolar Laparoscopic Coagulator (FDA Code: HFG / 884.416)

Identification. A unipolar endoscopic coagulator-cutter is a device designed to destroy tissue with high temperatures by directing a high frequency electrical current through the tissue between an energized probe and a grounding plate. It is used in female sterilization and in other operative procedures under endoscopic observation. This generic type of device may include the following accessories: an electrical generator, probes and electrical cables, and a patient grounding plate. This generic type of device does not include devices used to perform female sterilization under hysteroscopic observation.

Classification. Class II (performance standards).

TTI Medical, Elmed Inc., Fujinon, Inc., more...

Unscented Menstrual Pad (FDA Code: HHD / 884.5435)

Identification. An unscented menstrual pad is a device that is a pad made of cellulosic or synthetic material which is used to absorb menstrual or other vaginal discharge. This generic type of device includes sterile unscented menstrual pads used for medically indicated conditions, but does not include menstrual pads treated with scent (i.e., fragrance materials) or those with added antimicrobial agents or other drugs.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter only when the device is made of common cellulosic and synthetic material with an established safety profile. This exemption does not include the intralabial pads and reusable menstrual pads.

Halyard Health, Inc., Hospeco, Johnson & Johnson Hemisferica, S.A., more...

Unscented Menstrual Tampon (FDA Code: HEB / 884.547)

Identification. An unscented menstrual tampon is a device that is a plug made of cellulosic or synthetic material that is inserted into the vagina and used to absorb menstrual or other vaginal discharge. This generic type of device does not include menstrual tampons treated with scent (i.e., fragrance materials) or those with added antimicrobial agents or other drugs.

Classification. Class II (performance standards).

Halyard Health, Inc., Conway Mill, Natracare, LLC, more...

Urine Cytology Kits (FDA Code: OKY / 884.453)

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

Biosafe Supplies, LLC, Path-Tec, LLC

Used Breast Pumps
Philips Avent

Uterine Biopsy Punch
Copper intrauterine devices are small flexible devices made of copper that prevent pregnancy when inserted into a woman's uterus through her vagina. These are a safe and effective method of reversible, long-term contraception for most women. These devices do not affect breastfeeding, interfere with intercourse, or have hormonal side effects.
Elmed Inc., Codman & Shurtleff, Inc., Kmedic, more...

Uterine Clamp (FDA Code: HGC / 884.452)

Identification. An obstetric-gynecologic general manual instrument is one of a group of devices used to perform simple obstetric and gynecologic manipulative functions. This generic type of device consists of the following:

Classification. Class I (general controls). The devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 884.9.

KLS Martin, L.P., Vyaire Medical, Inc., Luxtec, more...

Uterine Curettes (FDA Code: HCY / 884.453)
Uterine Curettes is a surgical instrument shaped like a scoop or spoon and used to remove tissue or growths from a body cavity. This uterine curette is inserted into the uterine cavity and the wall of the cavity is scraped. The material scraped away from the wall is sending for pathological examination.

Identification. An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

Classification. (1) Class II (performance standards).

Cooper Surgical, Inc., KLS Martin, L.P., Marina Medical Instruments Inc., more...

Uterine Dilators
Uterine Dilators are designed for gynecological use. These are approximately 8 inches in length and double ended. These are made of solid steel, heavier and longer. Its one end is one French size larger than the other and the size is stamped on the dilator.
Codman & Shurtleff, Inc., Scientific Calibration Plus, Sklar Instruments, more...

Uterine Dilators Set
Codman & Shurtleff, Inc., Millennium Surgical Corp., Miltex, Inc., more...

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