Taiwan FDA registration b1720c7f775137a6b3f2e8b519dd59de
"Stryker" Zedent second generation acetabular system
TW: “史賽克”采登特第二代髖臼系統
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.·Registered Aug 01, 2021 – Aug 01, 2026ActiveRegistration details
- Analysis ID
- b1720c7f775137a6b3f2e8b519dd59de
- Customs Code
- DHA05603480201
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3358 Semi-restricted correlated metals/polymers/metals porous coating and cementless cement supplements
- Import Information
- import
Dates and status
- Registration Date
- Aug 01, 2021
- Expiry Date
- Aug 01, 2026
About this record
Access comprehensive regulatory information for "Stryker" Zedent second generation acetabular system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b1720c7f775137a6b3f2e8b519dd59de 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. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices