Taiwan FDA registration ed3a4f32fb8a632783757945344932b2
“Howmedica Osteonics” Restoration Acetabular Wedge Augment
TW: “好美得卡 奧斯得寧”金屬髖關節墊片
Registration details
- Analysis ID
- ed3a4f32fb8a632783757945344932b2
- License Form
- Ministry of Health Medical Device Import No. 031290
- Customs Code
- DHA05603129001
Company information
- Manufacturer
- HOWMEDICA OSTEONICS CORP.
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3358 Semi-restricted hip metal/polymer/metal porous coated cement-free compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 10, 2018
- Expiry Date
- Jul 10, 2028
About this record
Access comprehensive regulatory information for “Howmedica Osteonics” Restoration Acetabular Wedge Augment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed3a4f32fb8a632783757945344932b2 and manufactured by 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