Taiwan FDA registration 0bd913c4d05fb07ea14cbdc5125eaea2
"Stryker" Puhinchi adjustable annular bone implant
TW: “史賽克”普欣奇可調環骨植入物
Taiwan·Risk Class 2·Stryker Puerto Rico, LLC.;; STRYKER ENDOSCOPY·Registered Feb 13, 2019 – Feb 13, 2029ActiveRegistration details
- Analysis ID
- 0bd913c4d05fb07ea14cbdc5125eaea2
- Customs Code
- DHA05603224702
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
- Feb 13, 2019
- Expiry Date
- Feb 13, 2029
About this record
Access comprehensive regulatory information for "Stryker" Puhinchi adjustable annular bone implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0bd913c4d05fb07ea14cbdc5125eaea2 and manufactured by Stryker Puerto Rico, LLC.;; STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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