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"Schneihui" tibial articular surface pad - Taiwan Registration 245befac290b0b19581879038562ff82

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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245befac290b0b19581879038562ff82
Registration Details
Taiwan FDA Registration: 245befac290b0b19581879038562ff82
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Device Details

"Schneihui" tibial articular surface pad
TW: โ€œๅฒ่€่ผโ€่„›้ชจ้—œ็ฏ€้ข่ฅฏๅขŠ
Risk Class 2

Registration Details

245befac290b0b19581879038562ff82

DHA05602838400

Company Information

Product Details

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

N Orthopedics

N.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers

Contract manufacturing;; input

Dates and Status

Apr 25, 2016

Apr 25, 2026

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