"Konica Minolta" dry laser (unsterilized) - Taiwan Registration ce6e86d9d6d0b2809c93e23c915656c7
Access comprehensive regulatory information for "Konica Minolta" dry laser (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ce6e86d9d6d0b2809c93e23c915656c7 and manufactured by KONICA MINOLTA MEDICAL & GRAPHIC, INC.. The authorized representative in Taiwan is MEDEPOCH TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KONICA MINOLTA MEDICAL & GRAPHIC, INC., 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
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".
P Radiology Science
P.1840 Radiographic film
import
Dates and Status
May 08, 2007
May 08, 2012
May 05, 2014
Cancellation Information
Logged out
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"Konica Minolta" dry laser (unsterilized)
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
5295a5c1d69fac3230f591820adf09b8
1
"Konica Minolta" dry laser (unsterilized)
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
50e1f501ee8230b8cce855212bb5746d
1

