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“Argon” Retrievable Vena Cave Filter - Taiwan Registration 7745b649d26526f01b650bb24bff183e

Access comprehensive regulatory information for “Argon” Retrievable Vena Cave Filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7745b649d26526f01b650bb24bff183e and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..

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7745b649d26526f01b650bb24bff183e
Registration Details
Taiwan FDA Registration: 7745b649d26526f01b650bb24bff183e
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Device Details

“Argon” Retrievable Vena Cave Filter
TW: “雅客”可回收血栓過濾網
Risk Class 2
MD

Registration Details

7745b649d26526f01b650bb24bff183e

Ministry of Health Medical Device Import No. 030760

DHA05603076004

Company Information

United States

Product Details

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

E Cardiovascular devices

E3375 Cardiovascular endovascular filter

Imported from abroad

Dates and Status

Mar 12, 2018

Mar 12, 2028