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“DHEF” Matrix Retainer (Non-Sterile) - Taiwan Registration e8d3849c48623cebbf65f3a02e0f5d99

Access comprehensive regulatory information for “DHEF” Matrix Retainer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e8d3849c48623cebbf65f3a02e0f5d99 and manufactured by MEDIPAK MANUFACTURING CORP.. The authorized representative in Taiwan is DHEF 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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e8d3849c48623cebbf65f3a02e0f5d99
Registration Details
Taiwan FDA Registration: e8d3849c48623cebbf65f3a02e0f5d99
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Device Details

“DHEF” Matrix Retainer (Non-Sterile)
TW: “奇祁”基質保留器 (未滅菌)
Risk Class 1
MD

Registration Details

e8d3849c48623cebbf65f3a02e0f5d99

Ministry of Health Medical Device Import No. 020751

DHA09402075104

Company Information

Pakistan

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Aug 14, 2019

Aug 14, 2024