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"Pentax" electronic nasopharyngeal endoscope - Taiwan Registration e36918718367fba9c7896cc940d88425

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 e36918718367fba9c7896cc940d88425 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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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e36918718367fba9c7896cc940d88425
Registration Details
Taiwan FDA Registration: e36918718367fba9c7896cc940d88425
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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
Cancelled

Registration Details

e36918718367fba9c7896cc940d88425

DHA00602158100

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

Oct 18, 2010

Oct 18, 2020

Jun 22, 2022

Cancellation Information

Logged out

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