Taiwan FDA registration d8ebcec87c3ae8eaa76912d622bfe1e1
Clinical sample of "Gooddeka" (unsterilized)
TW: 〝好美得卡〞臨床用樣板 (未滅菌)
Registration details
- Analysis ID
- d8ebcec87c3ae8eaa76912d622bfe1e1
- Customs Code
- DHA04400151202
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Clinical templates consist of medical molds or probes that are used to select and configure implants for surgical plastic surgery or as guidelines before cutting tissue.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4800 Sample plate for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Oct 30, 2005
- Expiry Date
- Oct 30, 2025
About this record
Access comprehensive regulatory information for Clinical sample of "Gooddeka" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d8ebcec87c3ae8eaa76912d622bfe1e1 and manufactured by HOWMEDICA INTERNATIONAL S. DE R.L.;; 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