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"Pentax" electronic cystoscope - Taiwan Registration 49a106cd266ff8a40141485642d38013

Access comprehensive regulatory information for "Pentax" electronic cystoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49a106cd266ff8a40141485642d38013 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 PENTAX TOHOKU CO., LTD., 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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49a106cd266ff8a40141485642d38013
Registration Details
Taiwan FDA Registration: 49a106cd266ff8a40141485642d38013
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Device Details

"Pentax" electronic cystoscope
TW: โ€œ่ณ“ๅพ—ๅฃซโ€้›ปๅญๅผ่†€่ƒฑ้ก
Risk Class 2
Cancelled

Registration Details

49a106cd266ff8a40141485642d38013

DHA00602091406

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

Apr 20, 2010

Apr 20, 2020

Jun 22, 2022

Cancellation Information

Logged out

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