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Seeker group - Taiwan Registration d5fa0046277833b26d65611190e5df8a

Access comprehensive regulatory information for Seeker group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5fa0046277833b26d65611190e5df8a and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is EMIND BIOTECH MR CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including MAXXIM MEDICAL,ARGON DIVISION, ARROW INTERNATIONAL INC., and 2 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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d5fa0046277833b26d65611190e5df8a
Registration Details
Taiwan FDA Registration: d5fa0046277833b26d65611190e5df8a
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Device Details

Seeker group
TW: ๅฐŽๅผ•ๅ™จ็ต„
Risk Class 2

Registration Details

d5fa0046277833b26d65611190e5df8a

DHA00600702103

Company Information

United States

Product Details

vacuum

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

import

Dates and Status

Oct 18, 1993

Oct 18, 2028