Taiwan FDA registration 29776b3b79fef60f54d25bc9ffec3a32
“STERIS” V-PRO 60 Low Temperature Sterilization System
TW: “思泰瑞”汽化過氧化氫低溫滅菌鍋
Taiwan·Risk Class 2·MD·STERIS MEXICO, S. DE R. L. DE C.V.·Registered Apr 28, 2016 – Apr 28, 2026ExpiredRegistration details
- Analysis ID
- 29776b3b79fef60f54d25bc9ffec3a32
- License Form
- Ministry of Health Medical Device Import No. 028552
- Customs Code
- DHA05602855205
Company information
- Manufacturer
- STERIS MEXICO, S. DE R. L. DE C.V.
- Manufacturer Country
- Mexico
- Authorized Representative
- CHUNG TENG MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6860 Ethylene oxide gas sterilizer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 28, 2016
- Expiry Date
- Apr 28, 2026
About this record
Access comprehensive regulatory information for “STERIS” V-PRO 60 Low Temperature Sterilization System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 29776b3b79fef60f54d25bc9ffec3a32 and manufactured by STERIS MEXICO, S. DE R. L. DE C.V.. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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