Taiwan FDA registration 82498247f8a6c59fade63cf21853da7d

"Schneihui" meniscus repair system

TW: “史耐輝”半月板修補系統
Taiwan flagTaiwan·Risk Class 2·Ceterix Orthopaedics, Inc.;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Registered Nov 08, 2022 – Nov 08, 2027Active
Registration details
Analysis ID
82498247f8a6c59fade63cf21853da7d
Customs Code
DHA05603603405
Company information
Manufacturer Country
United States
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.5000 Non-absorbable polyethylene terephthalate sewing wire
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Nov 08, 2022
Expiry Date
Nov 08, 2027
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About this record

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 82498247f8a6c59fade63cf21853da7d and manufactured by Ceterix Orthopaedics, Inc.;; 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 ArthroCare Corporation;; SMITH & NEPHEW INC. ENDOSCOPY, 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.

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