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"Pentax" electronic nasopharyngeal endoscope - Taiwan Registration 7e80d856d315412bfab3a0088c2bee75

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 7e80d856d315412bfab3a0088c2bee75 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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7e80d856d315412bfab3a0088c2bee75
Registration Details
Taiwan FDA Registration: 7e80d856d315412bfab3a0088c2bee75
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Device Details

"Pentax" electronic nasopharyngeal endoscope
TW: "่ณ“ๅพ—ๅฃซ"้›ปๅญๅผ้ผปๅ’ฝๅ–‰ๅ…ง่ฆ–้ก
Risk Class 2
Cancelled

Registration Details

7e80d856d315412bfab3a0088c2bee75

DHA00601409803

Company Information

Product Details

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

G ENT Science

import

Dates and Status

Mar 09, 2006

Mar 09, 2016

May 28, 2018

Cancellation Information

Logged out

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