Taiwan FDA registration fd84807980d9f405912e399e88a2ece0
“Stryker” ICONIX SPEED Anchor
TW: “史賽克”艾康尼斯固定錨釘
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered Oct 03, 2021 – Oct 03, 2026ActiveRegistration details
- Analysis ID
- fd84807980d9f405912e399e88a2ece0
- License Form
- Ministry of Health Medical Device Import No. 034964
- Customs Code
- DHA05603496401
Company information
- Manufacturer
- STRYKER ENDOSCOPY
- Manufacturer Country
- 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 Orthopedic devices
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 03, 2021
- Expiry Date
- Oct 03, 2026
About this record
Access comprehensive regulatory information for “Stryker” ICONIX SPEED Anchor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd84807980d9f405912e399e88a2ece0 and manufactured by STRYKER ENDOSCOPY. 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