Taiwan FDA registration f5a9db88a8a5e74c8b4e5a27fb7e8b77

"Schneihui" laparoscopic instrument

TW: "史耐輝"腹腔鏡器械
Taiwan flagTaiwan·Risk Class 2·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Registered Nov 10, 2006 – Nov 10, 2021Cancelled
Registration details
Analysis ID
f5a9db88a8a5e74c8b4e5a27fb7e8b77
Customs Code
DHA00601740909
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
Nov 10, 2006
Expiry Date
Nov 10, 2021
Cancellation Date
Oct 12, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 f5a9db88a8a5e74c8b4e5a27fb7e8b77 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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