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“PENTAX” VIDEO PROCESSOR - Taiwan Registration 6baef64e7043a03c62e5b09a324391a5

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 6baef64e7043a03c62e5b09a324391a5 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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6baef64e7043a03c62e5b09a324391a5
Registration Details
Taiwan FDA Registration: 6baef64e7043a03c62e5b09a324391a5
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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

6baef64e7043a03c62e5b09a324391a5

Ministry of Health Medical Device Import No. 028206

DHA05602820602

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

Feb 24, 2016

Feb 24, 2021

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