Vitrolife, Inc.

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Web: http://www.vitrolife.com
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Address: 3601 South Inca Street, Englewood, Colorado 80110, USA
Phone: +1-(303)-762-1933, 866-848-7687 | Fax: +1-(303)-762-7084 | Map/Directions >>

Profile: Vitrolife, Inc. focuses on products and systems for the preparation, cultivation and storage of human cells, tissues & organs. We operate through the product areas such as fertility, transplantation and stem cell cultivation. We provide nutrient solutions and advanced one-time instruments such as needles & pipettes, for the treatment of human infertility. We offer solutions and systems to maintain tissue in optimal condition outside the body for the required time while waiting for transplantation. We also develop and market products for primarily clinical applications. We specialize in the field of cell and tissue technology. In product area stem cell cultivation, we work with media in order to be able to use stem cells for therapeutic purposes. We develop, manufacture and market media and instruments for assisted reproductive technology. We produce products and systems for organ transplantation, in order to minimize the ischemic reperfusion injuries by improving the solutions used for extra corporeal preservation of organs and tissues.

13 Products/Services (Click for related suppliers)

• Amniotic Fluid Sampler (FDA Code: HIO / 884.1550)

The amniotic fluid sampler (amniocentesis tray) is a collection of devices used to aspirate amniotic fluid from the amniotic sac via a transabdominal approach. Components of the amniocentesis tray include a disposable 3 inch 20 gauge needle with stylet and a 30 cc. syringe, as well as the various sample collection accessories, such as vials, specimen containers, medium, drapes, etc. The device is used at 16-18 weeks gestation for antepartum diagnosis of certain congenital abnormalities or anytime after 24 weeks gestation when used to assess fetal maturity.

• 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 Devices

• Assisted Reproduction Microtools (FDA Code: MQH / 884.6130)

Assisted reproduction microtools are pipettes or other devices used in the laboratory to denude, micromanipulate, hold, or transfer human gametes or embryos for assisted hatching, intracytoplasmic sperm injection (ICSI), or other assisted reproduction methods.

• 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.

• Electrosurgical Electrode Gel (FDA Code: JOT / 878.4400)

An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.

• In Vitro Fertilization/Embryo Transfer Equipment

• Medical Devices

• Pipettors, Pipettes

• Reproductive Media (FDA Code: MQL / 884.6180)

Reproductive media and supplement are products that are used for assisted reproduction procedures. Media include liquid and powder versions of various substances that come in direct physical contact with human gametes or embryos (including water, acid solutions used to treat gametes or embryos, rinsing solutions, sperm separation media, supplements, or oil used to cover the media) for the purposes of preparation, maintenance, transfer or storage. Supplements are specific reagents added to media to enhance specific properties of the media (e.g., proteins, sera, antibiotics, etc.).

• Syringe/Needle Combos

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

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.

• Ultrasonic Puls-Echo Scanner (FDA Code: IYO / 892.1560)

An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.