Taiwan FDA registration 2a9fc7ee5e5e9a309e658a48817f5c4e
“Stryker” LED Light Source
TW: “史賽克”醫用光源機
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered May 17, 2017 – May 17, 2027ActiveRegistration details
- Analysis ID
- 2a9fc7ee5e5e9a309e658a48817f5c4e
- License Form
- Ministry of Health Medical Device Import No. 029724
- Customs Code
- DHA05602972400
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)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 17, 2017
- Expiry Date
- May 17, 2027
About this record
Access comprehensive regulatory information for “Stryker” LED Light Source in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a9fc7ee5e5e9a309e658a48817f5c4e and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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