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“PENTAX” ELECTRO-SURGICAL KNIFE - Taiwan Registration e9606cc25b5d0e9f467086a6bb7e369c

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 e9606cc25b5d0e9f467086a6bb7e369c 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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e9606cc25b5d0e9f467086a6bb7e369c
Registration Details
Taiwan FDA Registration: e9606cc25b5d0e9f467086a6bb7e369c
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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

e9606cc25b5d0e9f467086a6bb7e369c

Ministry of Health Medical Device Import No. 028572

DHA05602857201

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 10, 2016

May 10, 2026

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