Taiwan FDA registration 228b51ef9deb6ba6f9c1c8d89c9f7b02
"Angelmed" Badley Levdan Schuller Vascular Stent System
TW: "安吉美爾德"巴德萊弗丹舒樂血管支架系統
Taiwan·Risk Class 3·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Registered Apr 23, 2012 – Apr 23, 2017CancelledRegistration details
- Analysis ID
- 228b51ef9deb6ba6f9c1c8d89c9f7b02
- Customs Code
- DHA00602332005
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
- Apr 23, 2012
- Expiry Date
- Apr 23, 2017
- Cancellation Date
- Jun 27, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Angelmed" Badley Levdan Schuller Vascular Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 228b51ef9deb6ba6f9c1c8d89c9f7b02 and manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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