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Intra-articular injection - Taiwan Registration cb3d1351a61c90a1ff4551391c0ae5f2

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 cb3d1351a61c90a1ff4551391c0ae5f2 and manufactured by SEIKAGAKU CORPORATION TAKAHAGI PLANT. The authorized representative in Taiwan is TCM BIOTECH INTERNATIONAL CORP..

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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cb3d1351a61c90a1ff4551391c0ae5f2
Registration Details
Taiwan FDA Registration: cb3d1351a61c90a1ff4551391c0ae5f2
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Device Details

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

Registration Details

cb3d1351a61c90a1ff4551391c0ae5f2

DHA00600881506

Company Information

Product Details

LIMITED TO PATIENTS WITH DEGENERATIVE KNEE ARTHRITIS PAIN WHO DO NOT RESPOND TO CONSERVATIVE NON-DRUG TREATMENT AND GENERAL ANALGESICS SUCH AS ACETAMINOPHEN ARE INEFFECTIVE; 102.12.25 EFFICACY CHANGE: AS DETAILED IN Chinese IMITATION SINGLE APPROVED VERSION, THE ORIGINAL 101.7.3 APPROVED Chinese IMITATION SINGLE APPROVED COPY IS RECYCLED AND SCRAPPED, THE FOLLOWING BLANK.

0399 Other artificial function substitutes

import

Dates and Status

Aug 21, 1998

Aug 21, 2028