Taiwan FDA registration 3f59cffaea060b180dc467dcaf4aa6f5

"Schneihui" manual arthroscopic equipment (sterilization)

TW: “史耐輝”手動式關節鏡器材 (滅菌)

Taiwan·Risk Class 1·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Registered May 22, 2009 – May 22, 2029Active

Registration details

Analysis ID: 3f59cffaea060b180dc467dcaf4aa6f5
Customs Code: DHA04400775503

Company information

Manufacturer: SMITH & NEPHEW INC. ENDOSCOPY DIVISION
Manufacturer Country: United States
Authorized Representative: SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)

Product details

Intended Use: Limited to the first level identification range of the classification and grading management method for medical equipment "Arthroscopy (N.1100)".
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.1100 Closing Lenses
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: May 22, 2009
Expiry Date: May 22, 2029

About this record

Access comprehensive regulatory information for "Schneihui" manual arthroscopic equipment (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f59cffaea060b180dc467dcaf4aa6f5 and manufactured by SMITH & NEPHEW INC. ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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