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Miquelon collagen matrix - Taiwan Registration 8b19bcd1054186950d1e7bb04d7d05ca

Access comprehensive regulatory information for Miquelon collagen matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8b19bcd1054186950d1e7bb04d7d05ca and manufactured by MAXIGEN BIOTECH INC.. The authorized representative in Taiwan is MAXIGEN BIOTECH INC..

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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8b19bcd1054186950d1e7bb04d7d05ca
Registration Details
Taiwan FDA Registration: 8b19bcd1054186950d1e7bb04d7d05ca
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Device Details

Miquelon collagen matrix
TW: ๅฏ†ๅ…‹้š†่† ๅŽŸ่›‹็™ฝๅŸบ่ณช
Risk Class 3

Registration Details

8b19bcd1054186950d1e7bb04d7d05ca

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4490 Absorbable hemostats and dressings

Domestic

Dates and Status

Aug 01, 2024

Sep 25, 2028