"Pentax" electronic duodenal endoscope - Taiwan Registration e2e3d8ba8a8ab1efe924bf8846fd08ff
Access comprehensive regulatory information for "Pentax" electronic duodenal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e2e3d8ba8a8ab1efe924bf8846fd08ff 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, 1 companies making similar products including PENTAX TOHOKU CO., LTD., and 1 recent registrations in the same category. 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
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology and urology
H.1500 Internal Scope and its accessories
import
Dates and Status
Apr 20, 2010
Apr 20, 2020
Jun 07, 2022
Cancellation Information
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