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Protective film fiber - Taiwan Registration fb4491db2d3485f3841a7a06c3517744

Access comprehensive regulatory information for Protective film fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb4491db2d3485f3841a7a06c3517744 and manufactured by BioTissue Holdings Inc.. The authorized representative in Taiwan is ORIENT EUROPHARMA 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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fb4491db2d3485f3841a7a06c3517744
Registration Details
Taiwan FDA Registration: fb4491db2d3485f3841a7a06c3517744
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Device Details

Protective film fiber
TW: ไฟ่ฆ–่†œ ็บ–
Risk Class 2

Registration Details

fb4491db2d3485f3841a7a06c3517744

DHA05603380706

Company Information

United States

Product Details

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

M Ophthalmology

M.9999 Miscellaneous

import

Dates and Status

Jul 06, 2020

Jul 06, 2025