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"Pentax" endoscopic image processor - Taiwan Registration 797179907a17568b9d30cc2408303a6c

Access comprehensive regulatory information for "Pentax" endoscopic image processor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 797179907a17568b9d30cc2408303a6c and manufactured by HOYA CORPORATION PENTAX YAMAGATA 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 YAMAGATA FACTORY, and 1 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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797179907a17568b9d30cc2408303a6c
Registration Details
Taiwan FDA Registration: 797179907a17568b9d30cc2408303a6c
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Device Details

"Pentax" endoscopic image processor
TW: โ€œ่ณ“ๅพ—ๅฃซโ€ๅ…ง่ฆ–้กๅฝฑๅƒ่™•็†ๅ™จ
Risk Class 2
Cancelled

Registration Details

797179907a17568b9d30cc2408303a6c

DHA00601831709

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Sep 12, 2007

Sep 12, 2022

Apr 12, 2024

Cancellation Information

Logged out

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