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TiO2Mesh Light Surgical mesh implant - Taiwan Registration 8f05c385f44be9334092d1bf9f1084fa

Access comprehensive regulatory information for TiO2Mesh Light Surgical mesh implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f05c385f44be9334092d1bf9f1084fa and manufactured by BIOCER ENTWICKLUNGS-GMBH. The authorized representative in Taiwan is HEALTH RIVER INC..

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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8f05c385f44be9334092d1bf9f1084fa
Registration Details
Taiwan FDA Registration: 8f05c385f44be9334092d1bf9f1084fa
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Device Details

TiO2Mesh Light Surgical mesh implant
TW: โ€œ็™พๆญ็‘Ÿโ€่ผ•้‡ๅž‹ไบŒๆฐงๅŒ–้ˆฆ็–ๆฐฃไฟฎ่ฃœ็ถฒ
Risk Class 2
MD

Registration Details

8f05c385f44be9334092d1bf9f1084fa

Ministry of Health Medical Device Import No. 036036

DHA05603603609

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I3300 Surgical mesh

Imported from abroad

Dates and Status

Nov 09, 2022

Nov 09, 2027