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Cenefom Ophthalmic Sponge - Taiwan Registration 5503108b592e81e58d9e2f6267d530ed

Access comprehensive regulatory information for Cenefom Ophthalmic Sponge in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5503108b592e81e58d9e2f6267d530ed and manufactured by CENEFOM CORP.. The authorized representative in Taiwan is CENEFOM CORP..

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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5503108b592e81e58d9e2f6267d530ed
Registration Details
Taiwan FDA Registration: 5503108b592e81e58d9e2f6267d530ed
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Device Details

Cenefom Ophthalmic Sponge
TW: Cenefom็œผ็ง‘็”จๆณกๆฃ‰
Risk Class 2
MD

Registration Details

5503108b592e81e58d9e2f6267d530ed

Ministry of Health Medical Device Manufacturing No. 006217

Company Information

Taiwan, Province of China

Product Details

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

M Ophthalmic devices

M4790 Sponge for ophthalmic use

Produced in Taiwan, China

Dates and Status

Oct 18, 2018

Oct 18, 2028