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Rebirth Pro2 Thrombus Aspiration Catheter - Taiwan Registration ba32d57ca8800c4081a6ffb8401c9378

Access comprehensive regulatory information for Rebirth Pro2 Thrombus Aspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba32d57ca8800c4081a6ffb8401c9378 and manufactured by Goodman Co., LTD. Yamanashi Facility. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..

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ba32d57ca8800c4081a6ffb8401c9378
Registration Details
Taiwan FDA Registration: ba32d57ca8800c4081a6ffb8401c9378
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Device Details

Rebirth Pro2 Thrombus Aspiration Catheter
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Risk Class 2
MD

Registration Details

ba32d57ca8800c4081a6ffb8401c9378

Ministry of Health Medical Device Import No. 034211

DHA05603421104

Company Information

Product Details

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

E Cardiovascular devices

E5150 Thrombectomy catheter

Imported from abroad

Dates and Status

Dec 08, 2020

Dec 08, 2025