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Aragan plus injection - Taiwan Registration d26f49542cbfe21ec8ea9625c5028f97

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 d26f49542cbfe21ec8ea9625c5028f97 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.

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d26f49542cbfe21ec8ea9625c5028f97
Registration Details
Taiwan FDA Registration: d26f49542cbfe21ec8ea9625c5028f97
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Device Details

Aragan plus injection
TW: ้กง็ซ‹่ˆ’้—œ้—œ็ฏ€ๅ…งๆณจๅฐ„ๅŠ‘
Risk Class 3
MD

Registration Details

d26f49542cbfe21ec8ea9625c5028f97

Ministry of Health Medical Device Import No. 036026

DHA05603602606

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N0003 Hyaluronic acid implants for the joint cavity

Imported from abroad

Dates and Status

Nov 02, 2022

Nov 02, 2027

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