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“Geistlich” Fibro-Gide Collagen Matrix - Taiwan Registration f0878a3c2e155e173b744817aff7ffb7

Access comprehensive regulatory information for “Geistlich” Fibro-Gide Collagen Matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0878a3c2e155e173b744817aff7ffb7 and manufactured by GEISTLICH PHARMA AG. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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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f0878a3c2e155e173b744817aff7ffb7
Registration Details
Taiwan FDA Registration: f0878a3c2e155e173b744817aff7ffb7
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Device Details

“Geistlich” Fibro-Gide Collagen Matrix
TW: “蓋氏”法博吉膠原蛋白基質
Risk Class 2
MD

Registration Details

f0878a3c2e155e173b744817aff7ffb7

Ministry of Health Medical Device Import No. 034009

DHA05603400909

Company Information

Switzerland

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

Oct 29, 2020

Oct 29, 2025