"Stryker" femoral head
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered Apr 26, 2017 – Apr 26, 2027Active- Analysis ID
- 92d7b12a5ee178f87be4a525960b6ec7
- Customs Code
- DHA05602970101
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3350 Semi-restricted cormium/polymer-like cement-type supplements
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Apr 26, 2017
- Expiry Date
- Apr 26, 2027
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Access comprehensive regulatory information for "Stryker" femoral head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92d7b12a5ee178f87be4a525960b6ec7 and manufactured by STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOWMEDICA OSTEONICS-STRYKER IRELAND, 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.