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"Pentax" electronic nasopharyngeal endoscope - Taiwan Registration 5111b2b3ba29280c4d7165fc17f24695

Access comprehensive regulatory information for "Pentax" 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 5111b2b3ba29280c4d7165fc17f24695 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, 1 companies making similar products including HOYA CORPORATION PENTAX MIYAGI FACTORY, and 2 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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5111b2b3ba29280c4d7165fc17f24695
Registration Details
Taiwan FDA Registration: 5111b2b3ba29280c4d7165fc17f24695
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Device Details

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

Registration Details

5111b2b3ba29280c4d7165fc17f24695

DHA00601876000

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

Mar 28, 2008

Mar 28, 2023

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