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"Pentax" endoscopic image processor - Taiwan Registration a22947075ebb915b68caedb8b8b86cd5

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 a22947075ebb915b68caedb8b8b86cd5 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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a22947075ebb915b68caedb8b8b86cd5
Registration Details
Taiwan FDA Registration: a22947075ebb915b68caedb8b8b86cd5
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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

a22947075ebb915b68caedb8b8b86cd5

DHA00601886300

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

May 22, 2008

May 22, 2018

Dec 13, 2019

Cancellation Information

Logged out

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