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"Asahi Kosell microcatheter" - Taiwan Registration a08b54988ed0ee9bafb87e51ab7f78f4

Access comprehensive regulatory information for "Asahi Kosell microcatheter" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a08b54988ed0ee9bafb87e51ab7f78f4 and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ASAHI INTECC(THAILAND) CO.,LTD, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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a08b54988ed0ee9bafb87e51ab7f78f4
Registration Details
Taiwan FDA Registration: a08b54988ed0ee9bafb87e51ab7f78f4
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Device Details

"Asahi Kosell microcatheter"
TW: โ€œๆœๆ—ฅโ€็ง‘ๅกž็ˆพๅพฎๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

a08b54988ed0ee9bafb87e51ab7f78f4

DHA00602126401

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 20, 2010

Jul 20, 2020

Jun 07, 2022

Cancellation Information

Logged out

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