Perouse Medical

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Contact: Patrick Sercomanens - International Marketing & Sales Manager
Web: http://www.perouse.com
E-Mail:
Address: SAS Route du Manoir, Ivry Le Temple 60173, France
Phone: +33-(3)-44 08 17 00 | Fax: +33-(3)-44 08 17 09 | Map/Directions >>

Profile: Perouse Medical specializes in cardiovascular surgery, oncology and interventional imaging fields. Our products for cardiovascular surgery include knitted and woven polyester vascular prostheses, balloon catheters, carotid shunts and vein strippers. Our implantable catheter port is flexible and with its reinforced outlet tube, and anti-bending system, it offers optimal safety. This non-thrombogenic, radio-opaque, silicone or polyurethane catheter, and connecting tubes with Huber needles are manufactured and supplied by us for use in oncology.

The company has revenues of USD 1-5 Million, has ~50 employees and is ISO 9001, CE certified.

FDA Registration Number: 3006942524
US Agent: Gordon Macfarlane / Icon Clinical Research
Phone: +1-(919)-873-8962 Fax: +1-(215)-699-6288 E-Mail:

23 Products/Services (Click for related suppliers)

• Angiographic Syringe

• Balloon Catheters

• Balloon Inflation Syringe (FDA Code: MAV / 870.1650)

An angiographic injector and syringe is a device that consists of a syringe and a high-pressure injector which are used to inject contrast material into the heart, great vessels, and coronary arteries to study the heart and vessels by x-ray photography.

• Cardiopulmonary Bypass Adaptor (FDA Code: DTL / 870.4290)

A cardiopulmonary bypass adaptor, stopcock, manifold, or fitting is a device used in cardiovascular diagnostic, surgical, and therapeutic applications to interconnect tubing, catheters, or other devices.

• Carotid Shunts

• Catheter Tip Blood Pressure Transducer (FDA Code: DXO / 870.2870)

A catheter tip pressure transducer is a device incorporated into the distal end of a catheter. When placed in the bloodstream, its mechanical or electrical properties change in relation to changes in blood pressure. These changes are transmitted to accessory equipment for processing.

• Diagnostic Intravascular Catheter (FDA Code: DQO / 870.1200)

An intravascular diagnostic catheter is a device used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels. Included in this generic device are right-heart catheters, left-heart catheters, and angiographic catheters, among others.

• General & Plastic Surgery Pediatric Catheter (FDA Code: GBN / 878.4200)

An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. Examples include irrigation and drainage catheters, pediatric catheters, peritoneal catheters (including dialysis), and other general surgical catheters. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. Examples of accessories include adaptors, connectors, and catheter needles.

• Huber Needles

• Implantable Intraosseous Port (FDA Code: MHC / 880.5570)

A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.

• Inflation Devices

• Infusion Needle

• Internal Non-Inflatable Breast Prosthesis (FDA Code: FTR / 878.3540)

• Intraocular Lens Guide (FDA Code: KYB / 886.4300)

An intraocular lens guide is a device intended to be inserted into the eye during surgery to direct the insertion of an intraocular lens and be removed after insertion is completed.

• Intravenous Administration Kit (FDA Code: FPA / 880.5440)

An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.

• Introducer Sets

• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)

• Surgical Needle Guide (FDA Code: GDF / 878.4800)

A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

• Synthetic/Biological Composite Vascular Graft (FDA Code: MAL / 870.3450)

A vascular graft prosthesis is an implanted device intended to repair, replace, or bypass sections of native or artificial vessels, excluding coronary or cerebral vasculature, and to provide vascular access. It is commonly constructed of materials such as polyethylene terephthalate and polytetrafluoroethylene, and it may be coated with a biological coating, such as albumin or collagen, or a synthetic coating, such as silicone. The graft structure itself is not made of materials of animal origin, including human umbilical cords.

• Syringe Injector

• Vascular Injection Systems

• Vein Strippers

• Vertebroplasty (Does Not Contain Cement) Injector (FDA Code: OAR / 888.4200)

A cement dispenser is a nonpowered syringe-like device intended for use in placing bone cement (888.3027) into surgical sites.