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Pentax Medical endoscopic image processor - Taiwan Registration 5e7d4afdd70b4ded29851a5c93272fae

Access comprehensive regulatory information for Pentax Medical endoscopic image processor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e7d4afdd70b4ded29851a5c93272fae and manufactured by DIGITAL ENDOSCOPY GMBH;; HOYA Corporation.. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Plexus Manufacturing Sdn. Bhd.;; HOYA Corporation., HOYA Corporation.;; PLEXUS MANUFACTURING SDN BHD., and 4 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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5e7d4afdd70b4ded29851a5c93272fae
Registration Details
Taiwan FDA Registration: 5e7d4afdd70b4ded29851a5c93272fae
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Device Details

Pentax Medical endoscopic image processor
TW: โ€œ่ณ“ๅพ—้†ซ็™‚โ€ๅ…ง่ฆ–้กๅฝฑๅƒ่™•็†ๅ™จ
Risk Class 2

Registration Details

5e7d4afdd70b4ded29851a5c93272fae

DHA05603286301

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Oct 10, 2019

Oct 10, 2029