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Address: Wilhelm-Hennemann-Str.9, Schwerin 19061, Germany
Phone: +49-(385)-395700
FDA Registration: 3003587189
Products: Catheter Connector (FDA Code:
GCD), Connecting Flexible Aspirating Tube (FDA Code:
BYY), General & Plastic Surgery Surgical Cannula (FDA Code:
GEA), Vacuum Collection Bottle (FDA Code:
KDQ), Water Jet Lavage Unit (FDA Code:
FQH), Lipoplasty Suction System (FDA Code:
MUU), ...
Human Med Ag is a manufacturer of medical devices.
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Address: Holtedam 1, Humlebaek DK-3050, Denmark
www.coloplast.com |
Send Inquiry |
Phone: +45-(0)-4911-1111
FDA Registration: 9610694 Year Established: 1957
Annual Revenues: USD 100-500 Million
Employee Count: ~7000
Quality: CE Certified
Products: Coude Catheter (FDA Code:
EZC), Balloon Retention Type Catheter (FDA Code:
EZL), Colostomy Pouch (FDA Code:
EZQ), Colostomy Appliance, Condom Urinary Catheter, Disposable Barium Enema Kit (FDA Code:
FCD), ...
Coloplast A/S develops products and services that make life easier for people with very personal & private medical conditions. Our business includes ostomy care, urology & continence care, and wound &
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Address: R. Corioland 1643, Sao Paulo, Sp 05047-001, Brazil
www.richter.com.br
Products: General Surgical Manual Instrument (FDA Code:
MDM), Lipoplasty Suction System (FDA Code:
MUU), ...
Richter Ltda. is a manufacturer of surgical instruments. Our product line includes retractors, optical fiber, hook, needle port, shears, zest saws, electrocoagulation, chisels, suction cannula, afasta
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Address: Z.I. De Lambermont 151, Rue Des Ormes, Verviers 4800, Belgium
www.euromi.com |
Send Inquiry |
Phone: +32-(87)-292222
FDA Registration: 3007697975 Quality: ISO 13485, ISO 9001 Certified
Products: Infiltration Handles, Mesotherapy, Dermatology Equipment, Dermatology Surgical Instrument, Micro Surgical Instrument for Plastic Surgery, Lipoplasty Suction System (FDA Code:
MUU), ...
Euromi S.A. specializes in the distribution and the manufacture of material of medicine, dermatology and plastic surgery. Our products include Lipomatic® Handpiece, Dermatic1, Dermatic2, translumi
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FDA Code / Regulation: MUU / 878.5040 A suction lipoplasty system is a device intended for aesthetic body contouring. The device consists of a powered suction pump (containing a microbial filter on the exhaust and a microbial in-line filter in the connecting tubing between the collection bottle and the safety trap), collection bottle, cannula, and connecting tube. The microbial filters, tubing, collection bottle, and cannula must be capable of being changed between patients. The powered suction pump has a motor with a minimum of 1/3 horsepower, a variable vacuum range from 0 to 29.9 inches of mercury, vacuum control valves to regulate the vacuum with accompanying vacuum gauges, a single or double rotary vane (with or without oil), a single or double diaphragm, a single or double piston, and a safety trap.
Classification. Class II (special controls). Consensus standards and labeling restrictions.