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“MegaGen” i-Gen Membrane - Taiwan Registration c5f53cb9015e311dbbb1097acd575e72

Access comprehensive regulatory information for “MegaGen” i-Gen Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5f53cb9015e311dbbb1097acd575e72 and manufactured by MEGAGEN IMPLANT CO., LTD.. The authorized representative in Taiwan is SUNRISER MEDICAL 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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c5f53cb9015e311dbbb1097acd575e72
Registration Details
Taiwan FDA Registration: c5f53cb9015e311dbbb1097acd575e72
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Device Details

“MegaGen” i-Gen Membrane
TW: “美佳”牙科鈦膜
Risk Class 2
MD

Registration Details

c5f53cb9015e311dbbb1097acd575e72

Ministry of Health Medical Device Import No. 032858

DHA05603285805

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F4760 bone plate

Imported from abroad

Dates and Status

Oct 10, 2019

Oct 10, 2024