Taiwan FDA registration 0bb2eaf9b272435059997bce8cdc6aa0
Betaferon auto-injector
TW: 貝他費隆自動注射器
Taiwan·Risk Class 2·OWEN MUMFORD LIMITED·Registered Sep 02, 2008 – Sep 02, 2023CancelledRegistration details
- Analysis ID
- 0bb2eaf9b272435059997bce8cdc6aa0
- Customs Code
- DHA00601919207
Company information
- Manufacturer
- OWEN MUMFORD LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- BAYER TAIWAN COMPANY 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)
- J.6920 注射針導引器
- Import Information
- import
Dates and status
- Registration Date
- Sep 02, 2008
- Expiry Date
- Sep 02, 2023
- Cancellation Date
- Nov 06, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Betaferon auto-injector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0bb2eaf9b272435059997bce8cdc6aa0 and manufactured by OWEN MUMFORD LIMITED. The authorized representative in Taiwan is BAYER TAIWAN COMPANY LTD..
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