Arterial embolization conduit - Taiwan Registration f64c62be4fec46e218f265e2f528108f
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 f64c62be4fec46e218f265e2f528108f and manufactured by AMERICAN BIOMED, INCORPORATED-CATHLAB DIVISION. The authorized representative in Taiwan is Swiss company Keith & Co., Ltd. Taipei Branch.
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including VERMED PHARMACEUTICAL LABORATORY, CLINICAL PLASTIC PRODUCTS S.A., 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.
Device Details
Product Details
The details are as detailed as the approved copy of the imitation label
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
import
Dates and Status
May 20, 1994
May 20, 1999
Aug 30, 2007
Cancellation Information
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Arterial embolization conduit
CLINICAL PLASTIC PRODUCTS S.A.
b84c3b1822d0b34baa66aff4f15ccd18
Arterial embolization conduit
DISPO MEDICA GMBH
e7eaa8c65bfeec3964053c55783d3134
Arterial embolization conduit
VERMED PHARMACEUTICAL LABORATORY
66ec016ef58f8d4aa2e43cfeab7fdf49