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"Pentax" electronic colonic endoscope - Taiwan Registration 4a8d71424d25ec9966aff4e1e717b4c5

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 4a8d71424d25ec9966aff4e1e717b4c5 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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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4a8d71424d25ec9966aff4e1e717b4c5
Registration Details
Taiwan FDA Registration: 4a8d71424d25ec9966aff4e1e717b4c5
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Device Details

"Pentax" electronic colonic endoscope
TW: โ€œ่ณ“ๅพ—ๅฃซโ€้›ปๅญ็ต่…ธๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

4a8d71424d25ec9966aff4e1e717b4c5

DHA00602066702

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

Mar 15, 2010

Mar 15, 2025

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