Taiwan FDA registration 8aabd2e6a006aacdd7c474ece747c1ec

Central catheter group

TW: 中央導管組
Taiwan flagTaiwan·Risk Class 2·ARGON MEDICAL DEVICES, INC.·Registered Oct 18, 1993 – Oct 18, 2023Expired
Registration details
Analysis ID
8aabd2e6a006aacdd7c474ece747c1ec
Customs Code
DHA00600701903
Company information
Manufacturer Country
United States
Authorized Representative
JENS MEDICAL CONSULTING LTD.
Product details
Intended Use
vacuum
Product Type (Level 1)
1300 Instruments for transfusion fluids
Import Information
import
Dates and status
Registration Date
Oct 18, 1993
Expiry Date
Oct 18, 2023
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About this record

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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