Taiwan FDA registration ea018187269c24deb966f30f518edec0

Hyjet intra-articular injection

TW: 海捷特關節腔注射劑

Taiwan·Risk Class 3·Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory·Registered Aug 19, 2008 – Aug 19, 2028Active

Registration details

Analysis ID: ea018187269c24deb966f30f518edec0
Customs Code: DHY00500249009

Company information

Manufacturer: Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory

Product details

Intended Use: 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.
Product Type (Level 1): N Orthopedics
Import Information: Domestic

Dates and status

Registration Date: Aug 19, 2008
Expiry Date: Aug 19, 2028

About this record

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.