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“PENTAX” ULTRASOUND UPPER G.I. VIDEOSCOPE - Taiwan Registration e90e943a807dfa02e649b3257242a7d3

Access comprehensive regulatory information for “PENTAX” ULTRASOUND UPPER G.I. VIDEOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e90e943a807dfa02e649b3257242a7d3 and manufactured by HOYA CORPORATION PENTAX MIYAGI 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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e90e943a807dfa02e649b3257242a7d3
Registration Details
Taiwan FDA Registration: e90e943a807dfa02e649b3257242a7d3
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Device Details

“PENTAX” ULTRASOUND UPPER G.I. VIDEOSCOPE
TW: “賓得”超音波電子式上消化道內視鏡
Risk Class 2
MD

Registration Details

e90e943a807dfa02e649b3257242a7d3

Ministry of Health Medical Device Import No. 028577

DHA05602857708

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

May 12, 2016

May 12, 2026