"Pentax" ultrasound electronic bronchoscope - Taiwan Registration cb75835b448863fc9eabf9f9172c4d19
Access comprehensive regulatory information for "Pentax" ultrasound electronic bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb75835b448863fc9eabf9f9172c4d19 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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cb75835b448863fc9eabf9f9172c4d19
Registration Details
Taiwan FDA Registration: cb75835b448863fc9eabf9f9172c4d19
Device Details
"Pentax" ultrasound electronic bronchoscope
TW: โ่ณๅพๅฃซโ่ถ
้ณๆณข้ปๅญๅผๆฏๆฐฃ็ฎก้ก
Risk Class 2

