Taiwan FDA registration 49f581f03651d7018603cb8972fea4e3
"Angimald" Budei Luminis vascular stents
TW: “安吉美爾德”巴德依．路明尼斯血管支架
Taiwan·Risk Class 2·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Registered Oct 01, 2007 – Oct 01, 2027ActiveRegistration details
- Analysis ID
- 49f581f03651d7018603cb8972fea4e3
- Customs Code
- DHA00601834807
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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2007
- Expiry Date
- Oct 01, 2027
About this record
Access comprehensive regulatory information for "Angimald" Budei Luminis vascular stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49f581f03651d7018603cb8972fea4e3 and manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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