"Meride" rectal dilator (unsterilized) - Taiwan Registration 037254699c3dd1fd7d565b024b394ab2
Access comprehensive regulatory information for "Meride" rectal dilator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 037254699c3dd1fd7d565b024b394ab2 and manufactured by MEDRAD, INC.. The authorized representative in Taiwan is Qiatai Enterprise Co., Ltd.
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
Product Details
Limited to the first level identification range of "rectal dilator (H.5450)" of the Measures for the Administration of Medical Devices.
H Gastroenterology and urology
H.5450 Rectal dilator
import
Dates and Status
Apr 24, 2013
Apr 24, 2018
Nov 15, 2019
Cancellation Information
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