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"Meritt" arteriovenous guide sheath - Taiwan Registration 01421827b2bd22f14e629e7fe0a4ff62

Access comprehensive regulatory information for "Meritt" arteriovenous guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01421827b2bd22f14e629e7fe0a4ff62 and manufactured by MERIT MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is Merit Medical Asia Company Limited Taiwan Branch (Hong Kong).

This page provides complete technical specifications, regulatory compliance details. 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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01421827b2bd22f14e629e7fe0a4ff62
Registration Details
Taiwan FDA Registration: 01421827b2bd22f14e629e7fe0a4ff62
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Device Details

"Meritt" arteriovenous guide sheath
TW: โ€œ็พŽ็‘ž็‰นโ€ๅ‹•้œ่„ˆๅฐŽๅผ•้ž˜
Risk Class 2

Registration Details

01421827b2bd22f14e629e7fe0a4ff62

DHA00602061203

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

import

Dates and Status

Feb 26, 2010

Feb 26, 2030