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"Schneihui" laparoscopic instrument - Taiwan Registration f5a9db88a8a5e74c8b4e5a27fb7e8b77

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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f5a9db88a8a5e74c8b4e5a27fb7e8b77
Registration Details
Taiwan FDA Registration: f5a9db88a8a5e74c8b4e5a27fb7e8b77
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Device Details

"Schneihui" laparoscopic instrument
TW: "ๅฒ่€่ผ"่…น่…”้กๅ™จๆขฐ
Risk Class 2
Cancelled

Registration Details

f5a9db88a8a5e74c8b4e5a27fb7e8b77

DHA00601740909

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Nov 10, 2006

Nov 10, 2021

Oct 12, 2023

Cancellation Information

Logged out

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