Taiwan FDA registration 8448cc2f306a3f18b9d79878a0da7a31
Breelib Inhalation System
TW: 備利吸入系統
Taiwan·Risk Class 2·MD·Vectura Group Ltd·Registered Jun 26, 2018 – Jun 26, 2028ActiveRegistration details
- Analysis ID
- 8448cc2f306a3f18b9d79878a0da7a31
- License Form
- Ministry of Health Medical Device Import No. 031202
- Customs Code
- DHA05603120201
Company information
- Manufacturer
- Vectura Group Ltd
- 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)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5630 Sprayer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 26, 2018
- Expiry Date
- Jun 26, 2028
About this record
Access comprehensive regulatory information for Breelib Inhalation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8448cc2f306a3f18b9d79878a0da7a31 and manufactured by Vectura Group Ltd. The authorized representative in Taiwan is BAYER TAIWAN COMPANY LTD..
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