Taiwan FDA registration ac9e1ef242b7fbc2d63145e5239452da
Diaphragmatic needle in the "Baylis" room
TW: “貝利斯”房中膈穿刺針
Taiwan·Risk Class 2·BAYLIS MEDICAL COMPANY INC.·Registered May 12, 2009 – May 12, 2014CancelledRegistration details
- Analysis ID
- ac9e1ef242b7fbc2d63145e5239452da
- Customs Code
- DHA00601984003
Company information
- Manufacturer
- BAYLIS MEDICAL COMPANY INC.
- Manufacturer Country
- Canada
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5175 Panectomy Conduit
- Import Information
- import
Dates and status
- Registration Date
- May 12, 2009
- Expiry Date
- May 12, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Diaphragmatic needle in the "Baylis" room in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac9e1ef242b7fbc2d63145e5239452da and manufactured by BAYLIS MEDICAL COMPANY INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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