Taiwan FDA registration 14d87cbbba890a7bfe7ae619903507c4
“Stryker” PEEK IntraLine Anchor
TW: “史賽克”英達來軟組織固定錨釘
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered Jul 31, 2014 – Jul 31, 2024ExpiredRegistration details
- Analysis ID
- 14d87cbbba890a7bfe7ae619903507c4
- License Form
- Ministry of Health Medical Device Import No. 026463
- Customs Code
- DHA05602646309
Company information
- Manufacturer
- STRYKER ENDOSCOPY
- 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)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 31, 2014
- Expiry Date
- Jul 31, 2024
About this record
Access comprehensive regulatory information for “Stryker” PEEK IntraLine Anchor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14d87cbbba890a7bfe7ae619903507c4 and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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