Taiwan FDA registration ac026aa0485ef7732c3dce53fb74dda0
“STERIS” AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
TW: “思泰瑞”低溫滅菌鍋
Registration details
- Analysis ID
- ac026aa0485ef7732c3dce53fb74dda0
- License Form
- Ministry of Health Medical Device Import No. 027935
- Customs Code
- DHA05602793503
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
- Nov 05, 2015
- Expiry Date
- Nov 05, 2025
About this record
Access comprehensive regulatory information for “STERIS” AMSCO V-PRO MAX 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 ac026aa0485ef7732c3dce53fb74dda0 and manufactured by Steris Mexico, S. de R.L. de C.V.. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS 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