Taiwan FDA registration f5b8caf9cc823ef593b0eb8fb8f34363

"Schneihui" mosaic arthroscopy manual instrument (sterilized)

TW: "史耐輝" 馬賽克關節鏡用手動器械 (滅菌)

Taiwan·Risk Class 1·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Registered Aug 18, 2006 – Aug 18, 2021Cancelled

Registration details

Analysis ID: f5b8caf9cc823ef593b0eb8fb8f34363
Customs Code: DHA04400507905

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 "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.1100 Closing Lenses
Import Information: import

Dates and status

Registration Date: Aug 18, 2006
Expiry Date: Aug 18, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Schneihui" mosaic arthroscopy manual instrument (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f5b8caf9cc823ef593b0eb8fb8f34363 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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