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“BIOTRONIK” ReCross OTW Dual Lumen GW Support Catheter - Taiwan Registration cf7d4612f31d975a87ece9e28b1e4b01

Access comprehensive regulatory information for “BIOTRONIK” ReCross OTW Dual Lumen GW Support Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cf7d4612f31d975a87ece9e28b1e4b01 and manufactured by IMDS Operations B.V.. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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cf7d4612f31d975a87ece9e28b1e4b01
Registration Details
Taiwan FDA Registration: cf7d4612f31d975a87ece9e28b1e4b01
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Device Details

“BIOTRONIK” ReCross OTW Dual Lumen GW Support Catheter
TW: “百多力” 力可過雙腔導線支撐導管
Risk Class 2
MD

Registration Details

cf7d4612f31d975a87ece9e28b1e4b01

Ministry of Health Medical Device Import No. 036628

DHA05603662808

Company Information

Netherlands

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Oct 10, 2023

Oct 10, 2028