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"Aiwei Medicine" Aiwei Modified Guide Tube - Taiwan Registration 7384d954420a19d58f7187c2a8db97d9

Access comprehensive regulatory information for "Aiwei Medicine" Aiwei Modified Guide Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7384d954420a19d58f7187c2a8db97d9 and manufactured by ALVIMEDICA TฤฐBBฤฐ Urunler SAN. AND EXTERNAL. T.C. Inc.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..

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7384d954420a19d58f7187c2a8db97d9
Registration Details
Taiwan FDA Registration: 7384d954420a19d58f7187c2a8db97d9
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Device Details

"Aiwei Medicine" Aiwei Modified Guide Tube
TW: โ€œ่‰พๅพฎ้†ซๅญธโ€่‰พๅพฎๆ”นๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

7384d954420a19d58f7187c2a8db97d9

DHA00602520209

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jul 08, 2013

Jul 08, 2018

Aug 05, 2022

Cancellation Information

Logged out

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