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"Pentax Medical" electronic nasopharyngeal endoscope - Taiwan Registration 06f97df0687d3fcd797761a2dc30ff37

Access comprehensive regulatory information for "Pentax Medical" electronic nasopharyngeal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06f97df0687d3fcd797761a2dc30ff37 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. 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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06f97df0687d3fcd797761a2dc30ff37
Registration Details
Taiwan FDA Registration: 06f97df0687d3fcd797761a2dc30ff37
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Device Details

"Pentax Medical" electronic nasopharyngeal endoscope
TW: โ€œ่ณ“ๅพ—้†ซ็™‚โ€้›ปๅญๅผ้ผปๅ’ฝๅ–‰ๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

06f97df0687d3fcd797761a2dc30ff37

DHA05603300904

Company Information

Product Details

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

G ENT Science

G.4760 Nasopharyngeal scopes (soft or rigid) and their accessories

import

Dates and Status

Nov 26, 2019

Nov 26, 2029