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“PENTAX” VIDEO PROCESSOR - Taiwan Registration d7d158a3592b9d6e0d83923f650ad9a9

Access comprehensive regulatory information for “PENTAX” VIDEO PROCESSOR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d7d158a3592b9d6e0d83923f650ad9a9 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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d7d158a3592b9d6e0d83923f650ad9a9
Registration Details
Taiwan FDA Registration: d7d158a3592b9d6e0d83923f650ad9a9
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Device Details

“PENTAX” VIDEO PROCESSOR
TW: “賓得”內視鏡影像處理器
Risk Class 2
MD

Registration Details

d7d158a3592b9d6e0d83923f650ad9a9

Ministry of Health Medical Device Import No. 025747

DHA05602574705

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

Dec 30, 2013

Dec 30, 2028

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