"Pentax" portable fiber optic hysteroscopy - Taiwan Registration da493b987053366cf40bcd45c0b108dd
Access comprehensive regulatory information for "Pentax" portable fiber optic hysteroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number da493b987053366cf40bcd45c0b108dd 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.
Free Database
Powered by Pure Global AI
89,000+ Devices
da493b987053366cf40bcd45c0b108dd
Registration Details
Taiwan FDA Registration: da493b987053366cf40bcd45c0b108dd
Device Details
"Pentax" portable fiber optic hysteroscopy
TW: "่ณๅพๅฃซ"ๅฏๆๅผๅ
็บๅญๅฎฎ้ก
Risk Class 2
Cancelled

