Taiwan FDA registration fbca55c01782ca31403ed28575c17190
“BeGraft” Peripheral Stent Graft System
TW: “潷葛睿孚”周邊覆膜支架系統
Taiwan·Risk Class 2·MD·Bentley InnoMed GmbH·Registered Feb 08, 2018 – Feb 08, 2028ActiveRegistration details
- Analysis ID
- fbca55c01782ca31403ed28575c17190
- License Form
- Ministry of Health Medical Device Import No. 030731
- Customs Code
- DHA05603073100
Company information
- Manufacturer
- Bentley InnoMed GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
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)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 08, 2018
- Expiry Date
- Feb 08, 2028
About this record
Access comprehensive regulatory information for “BeGraft” Peripheral Stent Graft System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fbca55c01782ca31403ed28575c17190 and manufactured by Bentley InnoMed GmbH. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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