Taiwan FDA registration 245befac290b0b19581879038562ff82

"Schneihui" tibial articular surface pad

TW: “史耐輝”脛骨關節面襯墊
Taiwan flagTaiwan·Risk Class 2·Smith & Nephew Orthopaedics, GmbH;; SMITH & NEPHEW, INC.·Registered Apr 25, 2016 – Apr 25, 2026Expired
Registration details
Analysis ID
245befac290b0b19581879038562ff82
Customs Code
DHA05602838400
Company information
Manufacturer Country
United States;;Germany
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Apr 25, 2016
Expiry Date
Apr 25, 2026
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About this record

Access comprehensive regulatory information for "Schneihui" tibial articular surface pad in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 245befac290b0b19581879038562ff82 and manufactured by Smith & Nephew Orthopaedics, GmbH;; SMITH & NEPHEW, INC.. 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., 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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