Pure Global

Aragan Plus Injection - Taiwan Registration 00200c9678cab5498aa4194ae88edbca

Access comprehensive regulatory information for Aragan Plus Injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 00200c9678cab5498aa4194ae88edbca and manufactured by Dongkwang Pharmaceutical Co., Ltd.. The authorized representative in Taiwan is UNIMED PHARMACEUTICAL ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Dongkwang Pharmaceutical Co., Ltd., and 1 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1 Competitors
1 Recent Registrations
00200c9678cab5498aa4194ae88edbca
Registration Details
Taiwan FDA Registration: 00200c9678cab5498aa4194ae88edbca
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Aragan Plus Injection
TW: ็Žป้œฒ้—œ็ฏ€ๅ…งๆณจๅฐ„ๅŠ‘
Risk Class 3
MD

Registration Details

00200c9678cab5498aa4194ae88edbca

Ministry of Health Medical Device Import No. 028812

DHA05602881205

Company Information

Korea, Republic of

Product Details

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

N Orthopedic devices

N0003 Hyaluronic acid implants for the joint cavity

Imported from abroad

Dates and Status

Aug 29, 2016

Aug 29, 2026

Companies Making Similar Products
Top companies providing products similar to "Aragan Plus Injection"