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"Pentax" electronic upper gastrointestinal endoscope - Taiwan Registration 02c2c35b209aa8455bb4e72eeddefc91

Access comprehensive regulatory information for "Pentax" electronic upper gastrointestinal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02c2c35b209aa8455bb4e72eeddefc91 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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02c2c35b209aa8455bb4e72eeddefc91
Registration Details
Taiwan FDA Registration: 02c2c35b209aa8455bb4e72eeddefc91
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Device Details

"Pentax" electronic upper gastrointestinal endoscope
TW: "่ณ“ๅพ—ๅฃซ" ้›ปๅญไธŠๆถˆๅŒ–้“ๅ…ง่ฆ–้ก
Risk Class 2
Cancelled

Registration Details

02c2c35b209aa8455bb4e72eeddefc91

DHA00601412700

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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