Taiwan FDA registration 221bf7b2d625aadaca915193ddbad1f9
"Angelmed" Bardei Luminis biliary stent
TW: “安吉美爾德”巴德依．路明尼斯膽道支架
Taiwan·Risk Class 2·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Registered Aug 27, 2007 – Aug 27, 2017CancelledRegistration details
- Analysis ID
- 221bf7b2d625aadaca915193ddbad1f9
- Customs Code
- DHA00601822402
Company information
- Manufacturer
- ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
- Manufacturer Country
- Germany
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5010 膽管用導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- Aug 27, 2007
- Expiry Date
- Aug 27, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Angelmed" Bardei Luminis biliary stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 221bf7b2d625aadaca915193ddbad1f9 and manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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