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Retaining membrane - Taiwan Registration 5de94508f452f49e3827add0d9047c41

Access comprehensive regulatory information for Retaining membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5de94508f452f49e3827add0d9047c41 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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5de94508f452f49e3827add0d9047c41
Registration Details
Taiwan FDA Registration: 5de94508f452f49e3827add0d9047c41
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Device Details

Retaining membrane
TW: ไฟ่ฆ–่†œ
Risk Class 2

Registration Details

5de94508f452f49e3827add0d9047c41

DHA05603161003

Company Information

United States

Product Details

This product can be used together to promote the healing of corneal conjunctival wounds or after the healing of infectious keratitis after surgery of general eyes, eyelids and eye sockets or in the acute and chronic stages of eye chemical burns. By covering the eyeball, this product provides a physical protection mechanism for the eyeball during the repair and restoration process.

M Ophthalmology

import

Dates and Status

Mar 26, 2019

Mar 26, 2029