Taiwan FDA registration 776bfc6689b3b03f945cc5b9e36a0a77
“Angiomed” Bard Venovo Venous Stent System
TW: “安吉美爾德”巴德維尼弗靜脈支架系統
Taiwan·Risk Class 2·MD·ANGIOMED GMBH & CO.MEDIZINTECHNIK KG·Registered Aug 14, 2017 – Aug 14, 2027ActiveRegistration details
- Analysis ID
- 776bfc6689b3b03f945cc5b9e36a0a77
- License Form
- Ministry of Health Medical Device Import No. 030010
- Customs Code
- DHA05603001000
Company information
- Manufacturer
- ANGIOMED GMBH & CO.MEDIZINTECHNIK KG
- Manufacturer Country
- Germany
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- This product is suitable for the treatment of stenosis and occlusion of the femoral vein.
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 14, 2017
- Expiry Date
- Aug 14, 2027
About this record
Access comprehensive regulatory information for “Angiomed” Bard Venovo Venous Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 776bfc6689b3b03f945cc5b9e36a0a77 and manufactured by ANGIOMED GMBH & CO.MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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