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“PENTAX” ELECTRO-SURGICAL KNIFE - Taiwan Registration f13394703e102df8f1703b1c66f0914f

Access comprehensive regulatory information for “PENTAX” 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 f13394703e102df8f1703b1c66f0914f 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, 1 companies making similar products including HOYA CORPORATION PENTAX YAMAGATA FACTORY, and 1 recent registrations in the same category. 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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f13394703e102df8f1703b1c66f0914f
Registration Details
Taiwan FDA Registration: f13394703e102df8f1703b1c66f0914f
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Device Details

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

Registration Details

f13394703e102df8f1703b1c66f0914f

Ministry of Health Medical Device Import No. 028349

DHA05602834908

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

Mar 30, 2016

Mar 30, 2026

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