Taiwan FDA registration 415c146e9b52d9ed08cf052452121115
“Stryker” Precision LED Light Source
TW: “史賽克”精準LED醫用光源機
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered Mar 31, 2018 – Mar 31, 2028ActiveRegistration details
- Analysis ID
- 415c146e9b52d9ed08cf052452121115
- License Form
- Ministry of Health Medical Device Import No. 031012
- Customs Code
- DHA05603101209
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
- Mar 31, 2018
- Expiry Date
- Mar 31, 2028
About this record
Access comprehensive regulatory information for “Stryker” Precision 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 415c146e9b52d9ed08cf052452121115 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