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"Pentax" ultrasound electronic upper gastrointestinal endoscope - Taiwan Registration 3a0a91cfd3b4226baeb1afbf176b0108

Access comprehensive regulatory information for "Pentax" ultrasound 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 3a0a91cfd3b4226baeb1afbf176b0108 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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3a0a91cfd3b4226baeb1afbf176b0108
Registration Details
Taiwan FDA Registration: 3a0a91cfd3b4226baeb1afbf176b0108
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Device Details

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

Registration Details

3a0a91cfd3b4226baeb1afbf176b0108

DHA00602062104

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 03, 2010

Mar 03, 2025