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“Unicare” CYTOFLEX Resorb - Taiwan Registration 033db9bd3f457110508ded8567bf6416

Access comprehensive regulatory information for “Unicare” CYTOFLEX Resorb in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 033db9bd3f457110508ded8567bf6416 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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033db9bd3f457110508ded8567bf6416
Registration Details
Taiwan FDA Registration: 033db9bd3f457110508ded8567bf6416
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Device Details

“Unicare” CYTOFLEX Resorb
TW: “憂尼卡”麗收骨可吸收式再生薄膜
Risk Class 2
MD

Registration Details

033db9bd3f457110508ded8567bf6416

Ministry of Health Medical Device Import No. 031053

DHA05603105300

Company Information

United States

Product Details

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

F Dental devices

F3930 Alveolar Restoration Materials

Imported from abroad

Dates and Status

Apr 24, 2018

Apr 24, 2028