Taiwan FDA registration 830bf35d23fbfb9bfe6fe9a5d9f7a953
“STERIS” Bowie Dick Test Pack
TW: “思泰瑞”抽真空測試包
Taiwan·Risk Class 2·MD·STERIS BIOLOGICAL OPERATIONS·Registered Aug 30, 2017 – Aug 30, 2022ExpiredRegistration details
- Analysis ID
- 830bf35d23fbfb9bfe6fe9a5d9f7a953
- License Form
- Ministry of Health Medical Device Import No. 030146
- Customs Code
- DHA05603014602
Company information
- Manufacturer
- STERIS BIOLOGICAL OPERATIONS
- Manufacturer Country
- United States
- 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)
- J2800 Sterilization Process Indicator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 30, 2017
- Expiry Date
- Aug 30, 2022
About this record
Access comprehensive regulatory information for “STERIS” Bowie Dick Test Pack in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 830bf35d23fbfb9bfe6fe9a5d9f7a953 and manufactured by STERIS BIOLOGICAL OPERATIONS. 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