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"Pentax" electronic colonic endoscope - Taiwan Registration a656ba58cd43360bef9126fd44b88c22

Access comprehensive regulatory information for "Pentax" electronic colonic endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a656ba58cd43360bef9126fd44b88c22 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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a656ba58cd43360bef9126fd44b88c22
Registration Details
Taiwan FDA Registration: a656ba58cd43360bef9126fd44b88c22
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Device Details

"Pentax" electronic colonic endoscope
TW: "่ณ“ๅพ—ๅฃซ" ้›ปๅญ็ต่…ธๅ…ง่ฆ–้ก
Risk Class 2
Cancelled

Registration Details

a656ba58cd43360bef9126fd44b88c22

DHA00601412608

Company Information

Product Details

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

H Gastroenterology and urology

import

Dates and Status

Mar 14, 2006

Mar 14, 2016

May 28, 2018

Cancellation Information

Logged out

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