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"Pentax" electronic upper gastrointestinal endoscope - Taiwan Registration 2a771434ff3f0ee746dc78e2d52c3928

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 2a771434ff3f0ee746dc78e2d52c3928 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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2a771434ff3f0ee746dc78e2d52c3928
Registration Details
Taiwan FDA Registration: 2a771434ff3f0ee746dc78e2d52c3928
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Device Details

"Pentax" electronic upper gastrointestinal endoscope
TW: โ€œ่ณ“ๅพ—ๅฃซโ€้›ปๅญไธŠๆถˆๅŒ–้“ๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

2a771434ff3f0ee746dc78e2d52c3928

DHA00601873909

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 24, 2008

Mar 24, 2028

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