"Pentax" electronic upper gastrointestinal endoscope - Taiwan Registration 02c2c35b209aa8455bb4e72eeddefc91
Access comprehensive regulatory information for "Pentax" electronic upper gastrointestinal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02c2c35b209aa8455bb4e72eeddefc91 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
H Gastroenterology and urology
import
Dates and Status
Mar 14, 2006
Mar 14, 2016
May 28, 2018
Cancellation Information
Logged out
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"Pentax" electronic upper gastrointestinal endoscope
HOYA CORPORATION PENTAX MIYAGI FACTORY
ea32437e3771e34be80488364ddfbda3
2
"Pentax" electronic upper gastrointestinal endoscope
HOYA CORPORATION PENTAX MIYAGI FACTORY
2a771434ff3f0ee746dc78e2d52c3928
2

