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"Schneihui" arthroscopy - Taiwan Registration 69d708d92febde78de1eb04197b2a526

Access comprehensive regulatory information for "Schneihui" arthroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69d708d92febde78de1eb04197b2a526 and manufactured by Henke-Sass, Wolf, GmbH;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Henke-Sass, Wolf, GmbH;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION, SMITH & NEPHEW INC. ENDOSCOPY DIVISION, and 2 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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69d708d92febde78de1eb04197b2a526
Registration Details
Taiwan FDA Registration: 69d708d92febde78de1eb04197b2a526
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Device Details

"Schneihui" arthroscopy
TW: โ€œๅฒ่€่ผโ€้—œ็ฏ€้ก
Risk Class 2

Registration Details

69d708d92febde78de1eb04197b2a526

DHA00602126602

Product Details

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

N Orthopedics

N.1100 Closing Lenses

Input;; Contract manufacturing

Dates and Status

Jul 20, 2010

Jul 20, 2025