"Stryker" Zeident second generation porous acetabular cup
Taiwan·Risk Class 2·Made (部分製程) in FRANCE;; STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered Aug 04, 2021 – Aug 04, 2026Active- Analysis ID
- 98eb3ec137eb905ce957ed58abc86b08
- Customs Code
- DHA05603480405
- Manufacturer Country
- Ireland;;France;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3353 Semi-restricted Segment Joints of Metallic/Ceramic/Polymer-like Bone Cement or Non-Porous Coating Cement-free Cement-type Supplements
- Import Information
- import
- Registration Date
- Aug 04, 2021
- Expiry Date
- Aug 04, 2026
Access comprehensive regulatory information for "Stryker" Zeident second generation porous acetabular cup in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98eb3ec137eb905ce957ed58abc86b08 and manufactured by Made (部分製程) in FRANCE;; 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. 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.