Taiwan FDA registration 4bd5c38cea97be58052f715f248fdf97
“STERIS” HarmonyAIR A-Series Surgical Lighting System
TW: “思泰瑞”哈莫寧艾爾A系列手術燈系統
Taiwan·Risk Class 2·MD·STERIS CORPORATION·Registered Jun 10, 2022 – Jun 10, 2027ActiveRegistration details
- Analysis ID
- 4bd5c38cea97be58052f715f248fdf97
- License Form
- Ministry of Health Medical Device Import No. 035573
- Customs Code
- DHA05603557304
Company information
- Manufacturer
- STERIS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRUST INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4580 Surgical light
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 10, 2022
- Expiry Date
- Jun 10, 2027
About this record
Access comprehensive regulatory information for “STERIS” HarmonyAIR A-Series Surgical Lighting System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4bd5c38cea97be58052f715f248fdf97 and manufactured by STERIS CORPORATION. The authorized representative in Taiwan is MEDTRUST INTERNATIONAL CO., LTD..
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