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"Schneihui" surgical sutures - Taiwan Registration 6f8ae11da509010ceb7a8b29bd299e27

Access comprehensive regulatory information for "Schneihui" surgical sutures in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f8ae11da509010ceb7a8b29bd299e27 and manufactured by ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SMITH & NEPHEW INC., ENDOSCOPY DIVISION, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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6f8ae11da509010ceb7a8b29bd299e27
Registration Details
Taiwan FDA Registration: 6f8ae11da509010ceb7a8b29bd299e27
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Device Details

"Schneihui" surgical sutures
TW: โ€œๅฒ่€่ผโ€ๆ‰‹่ก“็ธซ็ทš
Risk Class 2

Registration Details

6f8ae11da509010ceb7a8b29bd299e27

DHA05602971502

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.5000 Non-absorbable polyethylene terephthalate sewing wire

Input;; Contract manufacturing

Dates and Status

May 09, 2017

May 09, 2027

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