"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).
This page provides complete technical specifications, regulatory compliance details. 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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3a0a91cfd3b4226baeb1afbf176b0108
Registration Details
Taiwan FDA Registration: 3a0a91cfd3b4226baeb1afbf176b0108
Device Details
"Pentax" ultrasound electronic upper gastrointestinal endoscope
TW: โ่ณๅพๅฃซโ่ถ
้ณๆณข้ปๅญๅผไธๆถๅ้ๅ
ง่ฆ้ก
Risk Class 2

