"Pentax" electronic esophageal endoscope - Taiwan Registration 46c3a122c54f3118be0778ba719f5d9f
Access comprehensive regulatory information for "Pentax" electronic esophageal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46c3a122c54f3118be0778ba719f5d9f 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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46c3a122c54f3118be0778ba719f5d9f
Registration Details
Taiwan FDA Registration: 46c3a122c54f3118be0778ba719f5d9f
Device Details
"Pentax" electronic esophageal endoscope
TW: โ่ณๅพๅฃซโ้ปๅญๅผ้ฃ้ๅ
ง่ฆ้ก
Risk Class 2

