"Pentax" electronic nasopharyngeal endoscope - Taiwan Registration e36918718367fba9c7896cc940d88425
Access comprehensive regulatory information for "Pentax" electronic nasopharyngeal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e36918718367fba9c7896cc940d88425 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA CORPORATION PENTAX MIYAGI FACTORY, and 2 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
G ENT Science
G.4760 Nasopharyngeal scopes (soft or rigid) and their accessories
import
Dates and Status
Oct 18, 2010
Oct 18, 2020
Jun 22, 2022
Cancellation Information
Logged out
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"Pentax" electronic nasopharyngeal endoscope
HOYA CORPORATION PENTAX MIYAGI FACTORY
5111b2b3ba29280c4d7165fc17f24695
2
"Pentax" electronic nasopharyngeal endoscope
HOYA CORPORATION PENTAX MIYAGI FACTORY
7e80d856d315412bfab3a0088c2bee75
2

