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“PENTX” ELECTRO-SURGICAL KNIFE - Taiwan Registration b9a513bf3d549c51d679f7a12b40e295

Access comprehensive regulatory information for “PENTX” ELECTRO-SURGICAL KNIFE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b9a513bf3d549c51d679f7a12b40e295 and manufactured by HOYA CORPORATION PENTAX YAMAGATA FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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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b9a513bf3d549c51d679f7a12b40e295
Registration Details
Taiwan FDA Registration: b9a513bf3d549c51d679f7a12b40e295
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Device Details

“PENTX” ELECTRO-SURGICAL KNIFE
TW: “賓得”電燒手術刀器械
Risk Class 2
MD

Registration Details

b9a513bf3d549c51d679f7a12b40e295

Ministry of Health Medical Device Import No. 028578

DHA05602857800

Product Details

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

H Gastroenterology-urology devices

H4300 Electrocutors for endoscopes and accessories

Imported from abroad

Dates and Status

May 12, 2016

May 12, 2021