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Needle Blunt Blanks,Needle Catheter Suppliers & Manufacturers

1151 to 1200 of 2002 results  Page: << Previous 50 Results 20 21 22 23 [24] 25 26 27 28 29 30 >> Next 50 Results
Needle Blunt Blanks
Iscon Surgicals Limited

Needle Catheter
Novartis Nutrition Corporation, Shanghai Pudong Jinhuan Medical Products Co., Ltd.

Needle Counter
DeRoyal Industries, Atrion Medical Products, Inc., Xodus Medical, Inc., more...

Needle Destroyer
E Med Future, Inc., Bhasin Sons Private Limited, OriPlatform, more...

Needle Guide
CIVCO Medical Solutions, INRAD, Cook Endoscopy, more...

Needle Holder/Knot Tying Instrument
Cooper Surgical, Inc., Elmed Inc., Smith & Nephew Inc., more...

Needle Introducer & Knot Pusher
Conkin Surgical Instruments Ltd., Radium Accessories Service, Inc., 3by Ltd.

Needle Pulling Tissue Forceps
Rhein Medical Inc., Elmed Inc., Zimmer, Inc., more...

Needle-Type High-Frequency Epilator (FDA Code: KCW / 878.535)

Identification. A needle-type epilator is a device intended to destroy the dermal papilla of a hair by applying electric current at the tip of a fine needle that has been inserted close to the hair shaft, under the skin, and into the dermal papilla. The electric current may be high-frequency AC current, high-frequency AC combined with DC current, or DC current only.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9.

R.A. Fischer Co., Edge Systems Corporation, Elmed Inc., more...

Negative Pressure Wound Therapy Powered Suction Pump (FDA Code: OMP / 878.478)

Identification. A powered suction pump is a portable, AC-powered or compressed air-powered device intended to be used to remove infectious materials from wounds or fluids from a patient's airway or respiratory support system. The device may be used during surgery in the operating room or at the patient's bedside. The device may include a microbial filter.

Classification. Class II.

Marcon Group, Inc., APL Logistics Warehouse Management Services, Inc., Accuro Medical Products Llc, more...

Nephroscopes
Nephroscopes are instruments that are inserted percutaneously through a nephrostomy tract. They are used to access calculi in calyces that is not reached by the rigid instruments and frequently deflected into most of the intrarenal collecting system.
Cambrian Medical Inc., Gyrus ACMI, Pentax Medical Company, more...

Nerve and Muscle Stimulation
Zimmer MedizinSystems, Universal Medical Systems, Inc, M&C Specialties And Ivemsa

Nerve Holding Clamps
Millennium Surgical Corp.

Neuro-vascular Forceps
Codman & Shurtleff, Inc.

Neurological Accessories, Catheter Connectors
KCK Medical, R-Group International, Sophysa USA, Inc., more...

Neurological Percussor
BuyMSC, Adaptive Medical Concepts, Inc., Kaisers Surgical Instruments Pty Ltd

Neurological Stimulator
Nihon Kohden America, Inc., World Precision Instruments, Inc., Elmed Inc., more...

Neurophysiology Lasers
Lumenis Inc., GAM Laser, Inc., Deka Research & Development Corp., more...

Neurosurgery Craniotomes
Komet Medical

Neurosurgery Surgical Drapes
Depuy Orthopaedics, Inc., Allergan, Inc, Biomet, Inc, more...

Neurosurgery, Rotary Instruments
Medone Surgical, Inc., HMNGB Crocomed Technik Inc., Feather Safety Razor Co., Ltd., more...

Neurosurgical Instruments
HNM Medical, DePuy Orthopaedics, Inc, Spectra Medical Devices, Inc., more...

Nitinol Nonabsorbable Suture (FDA Code: NJU / 878.4495)

Identification. A stainless steel suture is a needled or unneedled nonabsorbable surgical suture composed of 316L stainless steel, in USP sizes 12-0 through 10, or a substantially equivalent stainless steel suture, intended for use in abdominal wound closure, intestinal anastomosis, hernia repair, and sternal closure.

Classification. Class II (special controls). The special control for this device is FDA's "Class II Special Controls Guidance Document: Surgical Sutures; Guidance for Industry and FDA." See 878.1(e) for the availability of this guidance document.

Medtronic Xomed Surgical Products, Inc

Nitrile Examination Disposable Gloves
AZReam, Inc., Adenna Inc., Glove Outlet LLC, more...

No Adhesive External Aesthetic Restoration Material (FDA Code: NOK / 878.38)

Identification. An external aesthetic restoration prosthesis is a device intended to be used to construct an external artificial body structure, such as an ear, breast, or nose. Usually the device is made of silicone rubber and it may be fastened to the body with an external prosthesis adhesive. The device is not intended to be implanted.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9. If the device is intended for use without an external prosthesis adhesive to fasten it to the body, the device is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, with respect to general requirements concerning records, and 820.198, with respect to complaint files.

Luxtec, Reforma, Llc, Shoney Scientific, Inc., more...

No Adhesive External Breast Prosthesis (FDA Code: NOJ / 878.38)

Identification. An external aesthetic restoration prosthesis is a device intended to be used to construct an external artificial body structure, such as an ear, breast, or nose. Usually the device is made of silicone rubber and it may be fastened to the body with an external prosthesis adhesive. The device is not intended to be implanted.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9. If the device is intended for use without an external prosthesis adhesive to fasten it to the body, the device is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, with respect to general requirements concerning records, and 820.198, with respect to complaint files.

2 Assist, LLC, American Breast Care Lp, Thuasne North America, more...

Non Aesthetic Collagen Implant (FDA Code: LMI)
Lacrimedics, Inc., Tipp Machine & Tool, Inc.

Non-Absorbable Gauze
DeRoyal Industries, Bioseal Medical Packaging Concepts, First Aid Bandage Co, more...

Non-Absorbable Sutures (FDA Code: GAO / 878.4495)
Non absorbable sutures are made from a variety of non biodegradable materials and encapsulated or walled off by fibroblasts. Non-absorbable sutures are made of materials which are not metabolized by the body and are used either on skin wound closure.
ArosurgicalT Instruments Corporation, Autosuture, Micrins, Inc., more...

Non-crushing Anterior Resection Clamps
Codman & Shurtleff, Inc.

Non-crushing Gastrointestinal Clamps
Codman & Shurtleff, Inc., Herger AG, Himalaya Trading Co. (Pvt) Ltd., more...

Non-Electrical Surgical Chair (FDA Code: FZK / 878.495)

Identification. A manual operating table and accessories and a manual operating chair and accessories are nonpowered devices, usually with movable components, intended to be used to support a patient during diagnostic examinations or surgical procedures.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9.

Alimed, Inc., Biofit Engineered Products, Hausted Patient Handling Systems, more...

Non-Illuminated Speculum (FDA Code: FXE / 878.18)

Identification. A speculum is a device intended to be inserted into a body cavity to aid observation. It is either nonilluminated or illuminated and may have various accessories.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9.

Medtronic Xomed Surgical Products, Inc, Vyaire Medical, Inc., Luxtec, more...

Non-Injectable Irrigating Solution
Baxter International Inc

Non-Invasive Tubing (FDA Code: GAZ / 880.674)

Identification. A vacuum-powered body fluid suction apparatus is a device used to aspirate, remove, or sample body fluids. The device is powered by an external source of vacuum. This generic type of device includes vacuum regulators, vacuum collection bottles, suction catheters and tips, connecting flexible aspirating tubes, rigid suction tips, specimen traps, noninvasive tubing, and suction regulators (with gauge).

Classification. Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 880.9.

Byron Medical, Inc., Autosuture, Vyaire Medical, Inc., more...

Non-invasive, Tissue Oximeter
Non-invasive, tissue oximeter is a device allowing the measurement of oxygenated and de-oxygenated hemoglobin concentrations in tissue. It works by emitting near infrared light into tissue at known distances from a collector. The collector light is measured and processed, and the absorption and scattering coefficients of the medium are determined. Once the absorption and scattering are determined, the assumption that hemoglobin is the only significant absorber is applied and the oxygenated and de-oxygenated hemoglobin concentrations are calculated.
Cambrian Medical Inc., ISS, Inc., Cardiac Science, Inc.

non-magnetic Towel clamp
Kendall-ltp

Non-Pneumatic Tourniquet (FDA Code: GAX / 878.59)

Identification. A nonpneumatic tourniquet is a device consisting of a strap or tubing intended to be wrapped around a patient's limb and tightened to reduce circulation.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9.

Spectrum Laboratories, Inc., Vyaire Medical, Inc., Cook Group Incorporated, more...

Non-Powered Portable Single Patient Suction Apparatus (FDA Code: GCY / 878.468)

Identification. A nonpowered, single patient, portable suction apparatus is a device that consists of a manually operated plastic, disposable evacuation system intended to provide a vacuum for suction drainage of surgical wounds.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 878.9.

Byron Medical, Inc., Depuy Orthopaedics, Inc., Autosuture, more...

Non-Remote Illuminator (FDA Code: FTF / 878.458)

Identification. A surgical lamp (including a fixture) is a device intended to be used to provide visible illumination of the surgical field or the patient.

Classification. Class II.

Bovie Medical Corporation, Medical Vision Industries, Inc., Bovie Medical Corp.

Non-Sterile Arm Board (With Cover) (FDA Code: NOD / 878.391)

Identification. A noninflatable extremity splint is a device intended to immobilize a limb or an extremity. It is not inflatable.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 878.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180 of this chapter, with respect to general requirements concerning records, and 820.198 of this chapter, with respect to complaint files.

Tarry Manufacturing, Pedicraft, Inc., The Soule Co., Inc., more...

Non-Sterile Cotton Tipped Applicator
Comfort Safety Products, Inc., Barnhardt Manufacturing Company

Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC / 878.391)

Identification. A noninflatable extremity splint is a device intended to immobilize a limb or an extremity. It is not inflatable.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 878.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180 of this chapter, with respect to general requirements concerning records, and 820.198 of this chapter, with respect to complaint files.

Luxtec, Heitco, Inc. Dba Dott Products, Faretec, Inc., more...

Non-sterile Gauze Roll Bandages
American Environmental Health & Safety, Cardinal Health, Inc., Dermapac, Inc., more...

Non-Sterile Tongue Depressors
Schueler & Company Inc, Clinimed, Inc., Bovie Medical Corporation, more...

Non-Stick Bandage Pads
American Environmental Health & Safety, Allmed Medical Products Co., Ltd.

Nonresorbable Gauze/sponge for External Use (FDA Code: NAB / 878.4014)

Identification. A nonresorbable gauze/sponge for external use is a sterile or nonsterile device intended for medical purposes, such as to be placed directly on a patient's wound to absorb exudate. It consists of a strip, piece, or pad made from open woven or nonwoven mesh cotton cellulose or a simple chemical derivative of cellulose. This classification does not include a nonresorbable gauze/sponge for external use that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in part 807, subpart E of this chapter subject to the limitations in 878.9.

Lifescience Plus, Inc., Medical Warehouse, Autosuture, more...

Obstetrical Instruments
U.S.E Surgical Instruments, NBD International, Inc., Mobilsonic, Inc., more...

Occlusive Wound and Burn Dressing (FDA Code: MGP)
Hollister Incorporated, Cook Group Incorporated, Zimmer, Inc., more...

Occlusive Wound Dressing (FDA Code: NAD / 878.402)

Identification. An occlusive wound dressing is a nonresorbable, sterile or non-sterile device intended to cover a wound, to provide or support a moist wound environment, and to allow the exchange of gases such as oxygen and water vapor through the device. It consists of a piece of synthetic polymeric material, such as polyurethane, with or without an adhesive backing. This classification does not include an occlusive wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in part 807, subpart E of this chapter subject to the limitations in 878.9.

Autosuture, Medtronic Xomed Surgical Products, Inc, Hollister Incorporated, more...

1151 to 1200 of 2002 results  Page: << Previous 50 Results 20 21 22 23 [24] 25 26 27 28 29 30 >> Next 50 Results
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