Taiwan FDA registration 2ac4a2907aaaded41c939799e84d094f

Aragan Injection

TW: 舒關關節內注射劑

Taiwan·Risk Class 3·MD·Dongkwang Pharmaceutical Co., Ltd.·Registered Nov 14, 2016 – Nov 14, 2026Active

Registration details

Analysis ID: 2ac4a2907aaaded41c939799e84d094f
License Form: Ministry of Health Medical Device Import No. 029043
Customs Code: DHA05602904302

Company information

Manufacturer: Dongkwang Pharmaceutical Co., Ltd.
Manufacturer Country: Korea, Republic of
Authorized Representative: UNIMED PHARMACEUTICAL ENTERPRISE CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N0003 Hyaluronic acid implants for the joint cavity
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 14, 2016
Expiry Date: Nov 14, 2026

About this record

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..

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