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Central catheter group - Taiwan Registration 8aabd2e6a006aacdd7c474ece747c1ec

Access comprehensive regulatory information for Central catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8aabd2e6a006aacdd7c474ece747c1ec and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAXXIM MEDICAL,ARGON DIVISION, 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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8aabd2e6a006aacdd7c474ece747c1ec
Registration Details
Taiwan FDA Registration: 8aabd2e6a006aacdd7c474ece747c1ec
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Device Details

Central catheter group
TW: ไธญๅคฎๅฐŽ็ฎก็ต„
Risk Class 2

Registration Details

8aabd2e6a006aacdd7c474ece747c1ec

DHA00600701903

Company Information

United States

Product Details

vacuum

1300 Instruments for transfusion fluids

import

Dates and Status

Oct 18, 1993

Oct 18, 2023

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