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Aragan Injection - Taiwan Registration 2ac4a2907aaaded41c939799e84d094f

Access comprehensive regulatory information for Aragan Injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2ac4a2907aaaded41c939799e84d094f 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. 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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2ac4a2907aaaded41c939799e84d094f
Registration Details
Taiwan FDA Registration: 2ac4a2907aaaded41c939799e84d094f
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Device Details

Aragan Injection
TW: ่ˆ’้—œ้—œ็ฏ€ๅ…งๆณจๅฐ„ๅŠ‘
Risk Class 3
MD

Registration Details

2ac4a2907aaaded41c939799e84d094f

Ministry of Health Medical Device Import No. 029043

DHA05602904302

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

Nov 14, 2016

Nov 14, 2026