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"Annica" multi-bone - Taiwan Registration 5766d8e6b1b936ae25cb733491e21297

Access comprehensive regulatory information for "Annica" multi-bone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5766d8e6b1b936ae25cb733491e21297 and manufactured by UNICARE BIOMEDICAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT 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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5766d8e6b1b936ae25cb733491e21297
Registration Details
Taiwan FDA Registration: 5766d8e6b1b936ae25cb733491e21297
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Device Details

"Annica" multi-bone
TW: "ๆ†‚ๅฐผๅก"ๅคšๆ‰ถ้ชจ
Risk Class 3

Registration Details

5766d8e6b1b936ae25cb733491e21297

DHA00601745108

Company Information

United States

Product Details

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

F Dentistry

F.3930 Alveolar repair materials

import

Dates and Status

Nov 24, 2006

Nov 24, 2026