ANGIOSCULPT

Company Name MAEVA CENTRE
Address BUSINESS PARK-EBENE
City, State / Province, ZIP / Postal Code REDUIT,
Country MP
FDA Owner/Operator Phone 230-466-3054
FDA Medical Specialty Code CV - Cardiovascular
FDA Product Code NWX
FDA Classification Name CATHETER, PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA), CUTTING/SCORING
FDA Device Classification Code Premarket Approval
FDA Regulation Number NULL
FDA Common Generic Name PTCA CATHETER
FDA Proprietary Device Name ANGIOSCULPT
FDA Owner / Operator Number 9060577
FDA Owner / Operator Name NATEC MEDICAL LTD
FDA Establishment Registration Number 3004415014
FDA Registered Establishment Name MAEVA CENTRE
FDA Operation Code(s) MM - Manufacturer

Competitors of MAEVA CENTRE

Our records indicate that the following medical device companyies may manufacture a similar device.

  Company Name Proprietary Device Name Common Generic Device Name
1 ANGIOSCORE, INC. ANGIOSCULPT SCORING BALLOON CATHETER PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY CATHETER


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