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“BeGraft” Peripheral Stent Graft System - Taiwan Registration fbca55c01782ca31403ed28575c17190

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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fbca55c01782ca31403ed28575c17190
Registration Details
Taiwan FDA Registration: fbca55c01782ca31403ed28575c17190
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Device Details

“BeGraft” Peripheral Stent Graft System
TW: “潷葛睿孚”周邊覆膜支架系統
Risk Class 2
MD

Registration Details

fbca55c01782ca31403ed28575c17190

Ministry of Health Medical Device Import No. 030731

DHA05603073100

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Feb 08, 2018

Feb 08, 2028