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Arterial embolization conduit - Taiwan Registration b84c3b1822d0b34baa66aff4f15ccd18

Access comprehensive regulatory information for Arterial embolization conduit in Taiwan's medical device market through Pure Global AI's free database. is registered under number b84c3b1822d0b34baa66aff4f15ccd18 and manufactured by CLINICAL PLASTIC PRODUCTS S.A.. The authorized representative in Taiwan is MAX-ALLIED CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including VERMED PHARMACEUTICAL LABORATORY, DISPO MEDICA GMBH, and 3 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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b84c3b1822d0b34baa66aff4f15ccd18
Registration Details
Taiwan FDA Registration: b84c3b1822d0b34baa66aff4f15ccd18
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Device Details

Arterial embolization conduit
TW: ๅ‹•่„ˆๆ “ๅกžๆธ…้™คๅฐŽ็ฎก
Cancelled

Registration Details

b84c3b1822d0b34baa66aff4f15ccd18

DHA00600611303

Company Information

Switzerland

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Nov 01, 1990

Nov 01, 2000

Dec 14, 2004

Cancellation Information

Logged out

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