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Intra-articular injection - Taiwan Registration 07a1bc935638d8a6334e1a7a7ae5fe43

Access comprehensive regulatory information for 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 07a1bc935638d8a6334e1a7a7ae5fe43 and manufactured by MAXIGEN BIOTECH INC.. The authorized representative in Taiwan is MAXIGEN BIOTECH INC..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including MAXIGEN BIOTECH INC., Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory, and 5 recent registrations in the same category. 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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07a1bc935638d8a6334e1a7a7ae5fe43
Registration Details
Taiwan FDA Registration: 07a1bc935638d8a6334e1a7a7ae5fe43
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Device Details

Intra-articular injection
TW: ๅฎ‰็ฏ€็›Š ้—œ็ฏ€ๅ…งๆณจๅฐ„ๅŠ‘
Risk Class 3

Registration Details

07a1bc935638d8a6334e1a7a7ae5fe43

DHY00500217300

Company Information

Taiwan, Province of China

Product Details

As a treatment for patients with degenerative knee arthritis pain, it is limited to conservative non-pharmacological treatments and when general analgesics (eg, Acetaminophen) do not respond.

N Orthopedics

Domestic

Dates and Status

Oct 10, 2019

Aug 22, 2026