Laboratoires Prodimed

Address: 4 Rue De L'europe Zi, Neuilly En Thelle 60530, France
Phone: 33-992-66596 | Map/Directions >>

Profile: Laboratoires Prodimed specializes is in the production of hysterosraphy insufflator, intrauterine catheter, endometrial suction curette and catheter.

FDA Registration Number: 9612445
US Agent: Rene Van De Zande / Emergo Global Representation Llc
Phone: +1-(512)-327-9997 Fax: +1-(512)-327-9998 E-Mail:

12 Products/Services (Click for related suppliers)

• Assisted Reproduction Catheter (FDA Code: MQF / 884.6110)

Assisted reproduction catheters are devices used in in vitro fertilization (IVF), gamete intrafallopian transfer (GIFT), or other assisted reproduction procedures to introduce or remove gametes, zygote(s), preembryo(s), and/or embryo(s) into or from the body. This generic type of device may include catheters, cannulae, introducers, dilators, sheaths, stylets, and component parts.

• Assisted Reproduction Needle (FDA Code: MQE / 884.6100)

Assisted reproduction needles are devices used in in vitro fertilization (IVF), gamete intrafallopian transfer (GIFT), or other assisted reproduction procedures to obtain gametes from the body or introduce gametes, zygote(s), preembryo(s) and/or embryo(s) into the body. This generic type of device may include a single or double lumen needle and component parts, including needle guides, such as those used with ultrasound.

• Cancer Screening, Endometrial Suction Curettes

• Cervical Caps (FDA Code: HDR / 884.5250)

A cervical cap is a flexible cuplike receptacle that fits over the cervix to collect menstrual flow or to aid artificial insemination. This generic type of device is not for contraceptive use.

• Cytology Cervical Spatula (FDA Code: HHT / 884.4530)

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:

• Endometrial Suction Curette and Accessories (FDA Code: HHK / 884.1175)

An endometrial suction curette is a device used to remove material from the uterus and from the mucosal lining of the uterus by scraping and vacuum suction. This device is used to obtain tissue for biopsy or for menstrual extraction. This generic type of device may include catheters, syringes, and tissue filters or traps.

• Fertility Products, Endometrial Suction Curette

• Hysteroscopic Insufflator (FDA Code: HIG / 884.1700)

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.

• Intrauterine Catheter and Introducer (FDA Code: HGS / 884.2700)

An intrauterine pressure monitor is a device designed to detect and measure intrauterine and amniotic fluid pressure with a catheter placed transcervically into the uterine cavity. The device is used to monitor intensity, duration, and frequency of uterine contractions during labor. This generic type of device may include the following accessories: signal analysis and display equipment, patient and equipment supports, and component parts.

• Intrauterine Insemination Cannula (FDA Code: MFD / 884.5250)

• Oocyte Aspiration Needle

• Synthetic Cell and Tissue Culture Media and Components (FDA Code: KIT / 864.2220)

Synthetic cell and tissue culture media and components are substances that are composed entirely of defined components (e.g., amino acids, vitamins, inorganic salts) that are essential for the survival and development of cell lines of humans and other animals. This does not include tissue culture media for human ex vivo tissue and cell culture processing applications as described in 876.5885 of this chapter.