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"Pentax" electronic colonic endoscope - Taiwan Registration 73f1172099deafa82bc951c4080cab5e

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 73f1172099deafa82bc951c4080cab5e 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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73f1172099deafa82bc951c4080cab5e
Registration Details
Taiwan FDA Registration: 73f1172099deafa82bc951c4080cab5e
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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

73f1172099deafa82bc951c4080cab5e

DHA00601913406

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

Jul 29, 2008

Jul 29, 2028

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