Taiwan FDA registration b90a83a75cdf9ace8b03d0e2f764af58

"Schneihui" laparoscopic instrument

TW: “史耐輝”腹腔鏡器械
Taiwan flagTaiwan·Risk Class 2·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Registered Mar 15, 2007 – Mar 15, 2017Cancelled
Registration details
Analysis ID
b90a83a75cdf9ace8b03d0e2f764af58
Customs Code
DHA00601794201
Company information
Manufacturer Country
United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.1500 Internal Scope and its accessories
Import Information
import
Dates and status
Registration Date
Mar 15, 2007
Expiry Date
Mar 15, 2017
Cancellation Date
Nov 15, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Schneihui" laparoscopic instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b90a83a75cdf9ace8b03d0e2f764af58 and manufactured by 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, 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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