Taiwan FDA registration c5d2367e734215d10094c3925bf40795
“Maquet” Hemashield Platinum Woven Double Velour Vascular Grafts
TW: “邁柯唯”白金雙重絲絨人工血管
Taiwan·Risk Class 2·MD·INTERVASCULAR SAS·Registered Jul 07, 2017 – Jul 07, 2027ActiveRegistration details
- Analysis ID
- c5d2367e734215d10094c3925bf40795
- License Form
- Ministry of Health Medical Device Import No. 029959
- Customs Code
- DHA05602995901
Company information
- Manufacturer
- INTERVASCULAR SAS
- Manufacturer Country
- France
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E3450 Vascular graft supplement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 07, 2017
- Expiry Date
- Jul 07, 2027
About this record
Access comprehensive regulatory information for “Maquet” Hemashield Platinum Woven Double Velour Vascular Grafts in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5d2367e734215d10094c3925bf40795 and manufactured by INTERVASCULAR SAS. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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