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Hyjet intra-articular injection - Taiwan Registration ea018187269c24deb966f30f518edec0

Access comprehensive regulatory information for Hyjet intra-articular injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ea018187269c24deb966f30f518edec0 and manufactured by Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory. The authorized representative in Taiwan is Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory.

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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ea018187269c24deb966f30f518edec0
Registration Details
Taiwan FDA Registration: ea018187269c24deb966f30f518edec0
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Device Details

Hyjet intra-articular injection
TW: ๆตทๆท็‰น้—œ็ฏ€่…”ๆณจๅฐ„ๅŠ‘
Risk Class 3

Registration Details

ea018187269c24deb966f30f518edec0

DHY00500249009

Company Information

Product Details

It is limited to patients with degenerative knee arthritis pain who do not respond to conservative non-drug treatment and general analgesics such as Acetaminophen.

N Orthopedics

Domestic

Dates and Status

Aug 19, 2008

Aug 19, 2028