"Schneihui" meniscus repair system - Taiwan Registration 85279e1a550609a6303411568991ad76
Access comprehensive regulatory information for "Schneihui" meniscus repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 85279e1a550609a6303411568991ad76 and manufactured by ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY, Ceterix Orthopaedics, Inc.;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION, and 3 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.
Device Details
Registration Details
85279e1a550609a6303411568991ad76
DHA05603538605
Product Details
Details are as detailed as approved Chinese instructions
I General, Plastic Surgery and Dermatology
I.5000 Non-absorbable polyethylene terephthalate sewing wire
Input;; Contract manufacturing
Dates and Status
Apr 15, 2022
Apr 15, 2027
"Schneihui" meniscus repair system
Ceterix Orthopaedics, Inc.;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION
82498247f8a6c59fade63cf21853da7d
2
"Schneihui" meniscus repair system
ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY
26584c4e7076ad7eda87c4f9bf6544d3
2
"Schneihui" meniscus repair system
ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY
01d3e5ca66ea3c8a82d68f92dc04209a
2

