“PENTAX” VIDEO DUODENOSCOPE - Taiwan Registration bfeb730fed9c8abc59c9321132b87476
Access comprehensive regulatory information for “PENTAX” VIDEO DUODENOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bfeb730fed9c8abc59c9321132b87476 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.
Device Details
Registration Details
bfeb730fed9c8abc59c9321132b87476
Ministry of Health Medical Device Import No. 027130
DHA05602713000
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology-urology devices
H1500 endoscope and accessories
Imported from abroad
Dates and Status
Mar 10, 2015
Mar 10, 2025

