“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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Device Details
Registration Details
fbca55c01782ca31403ed28575c17190
Ministry of Health Medical Device Import No. 030731
DHA05603073100
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

