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“POLYDIAGNOST” POLYSCOPE - Taiwan Registration fff67cb0e8976f48dc445dfc51f89c37

Access comprehensive regulatory information for “POLYDIAGNOST” POLYSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fff67cb0e8976f48dc445dfc51f89c37 and manufactured by PolyDiagnost GmbH. The authorized representative in Taiwan is REVO LASER CORPORATION.

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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fff67cb0e8976f48dc445dfc51f89c37
Registration Details
Taiwan FDA Registration: fff67cb0e8976f48dc445dfc51f89c37
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Device Details

“POLYDIAGNOST” POLYSCOPE
TW: “波力”軟式內視鏡套組
Risk Class 2
MD

Registration Details

fff67cb0e8976f48dc445dfc51f89c37

Ministry of Health Medical Device Import No. 033744

DHA05603374408

Company Information

Germany

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Jul 21, 2020

Jul 21, 2025