Taiwan FDA registration a5c58d91cb4fbc399a5088ecb020fce1
"Stryker" integrated cutting and RF output energy supply system
TW: “史賽克”綜合切除與射頻輸出能量供應系統
Taiwan·Risk Class 2·STRYKER ENDOSCOPY·Registered Jun 20, 2017 – Jun 20, 2027ActiveRegistration details
- Analysis ID
- a5c58d91cb4fbc399a5088ecb020fce1
- Customs Code
- DHA05602979803
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)
- I General, Plastic Surgery and Dermatology; N Orthopedics
- Product Type (Level 2)
- N.1100 Closing Lenses;; I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Jun 20, 2017
- Expiry Date
- Jun 20, 2027
About this record
Access comprehensive regulatory information for "Stryker" integrated cutting and RF output energy supply system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5c58d91cb4fbc399a5088ecb020fce1 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