Taiwan FDA registration 1019e9c11ac31e7c7a2c7e6f7347e988
"Stryker" anterior cruciate ligament interface fixing screw
TW: “史賽克”前十字韌帶界面固定螺釘
Taiwan·Risk Class 2·Stryker Puerto Rico, LLC.;; STRYKER ENDOSCOPY·Registered Jan 20, 2014 – Jan 20, 2029ActiveRegistration details
- Analysis ID
- 1019e9c11ac31e7c7a2c7e6f7347e988
- Customs Code
- DHA05602576303
Company information
- Manufacturer
- Stryker Puerto Rico, LLC.;; STRYKER ENDOSCOPY
- Manufacturer Country
- Puerto Rico;;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
- Jan 20, 2014
- Expiry Date
- Jan 20, 2029
About this record
Access comprehensive regulatory information for "Stryker" anterior cruciate ligament interface fixing screw in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1019e9c11ac31e7c7a2c7e6f7347e988 and manufactured by Stryker Puerto Rico, LLC.;; 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