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Gonafen injection needle - Taiwan Registration 9f1f67fd9ef844c039f44f2e41cca4d0

Access comprehensive regulatory information for Gonafen injection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f1f67fd9ef844c039f44f2e41cca4d0 and manufactured by TERUMO EUROPE N.V.. The authorized representative in Taiwan is MERCK LTD..

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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9f1f67fd9ef844c039f44f2e41cca4d0
Registration Details
Taiwan FDA Registration: 9f1f67fd9ef844c039f44f2e41cca4d0
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Device Details

Gonafen injection needle
TW: ๆžœ็ด่Šฌๆณจๅฐ„้‡
Risk Class 2
Cancelled

Registration Details

9f1f67fd9ef844c039f44f2e41cca4d0

DHA00601270208

Company Information

Belgium

Product Details

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

J General hospital and personal use equipment

import

Dates and Status

Oct 14, 2005

Oct 14, 2015

Apr 13, 2018

Cancellation Information

Logged out

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