Taiwan FDA registration 7d582e92c9ce8f6986ec23fea390357a
"Stryker" Indah titanium alloy fixed anchors
TW: “史賽克”英達來鈦合金固定錨釘
Taiwan·Risk Class 2·STRYKER ENDOSCOPY·Registered Sep 26, 2014 – Sep 26, 2024ExpiredRegistration details
- Analysis ID
- 7d582e92c9ce8f6986ec23fea390357a
- Customs Code
- DHA05602662002
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 Orthopedics
- Product Type (Level 2)
- N.3040 Smooth or spiral metal bone fixations
- Import Information
- import
Dates and status
- Registration Date
- Sep 26, 2014
- Expiry Date
- Sep 26, 2024
- Cancellation Date
- Sep 19, 2024
About this record
Access comprehensive regulatory information for "Stryker" Indah titanium alloy fixed anchors in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d582e92c9ce8f6986ec23fea390357a 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