Taiwan FDA registration 00e0c4a5eaa16283b06cac554557b52e
“Stryker” Precision AC Camera System
TW: “史賽克”可滅菌式精準醫用影像攝像系統
Taiwan·Risk Class 2·MD·STRYKER ENDOSCOPY·Registered Oct 13, 2023 – Oct 13, 2028ActiveRegistration details
- Analysis ID
- 00e0c4a5eaa16283b06cac554557b52e
- License Form
- Ministry of Health Medical Device Import No. 036804
- Customs Code
- DHA05603680402
Company information
- Manufacturer
- STRYKER ENDOSCOPY
- Manufacturer Country
- United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 13, 2023
- Expiry Date
- Oct 13, 2028
About this record
Access comprehensive regulatory information for “Stryker” Precision AC Camera System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 00e0c4a5eaa16283b06cac554557b52e and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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