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"Konica Minolta" dry laser (unsterilized) - Taiwan Registration 50e1f501ee8230b8cce855212bb5746d

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 50e1f501ee8230b8cce855212bb5746d 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.

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50e1f501ee8230b8cce855212bb5746d
Registration Details
Taiwan FDA Registration: 50e1f501ee8230b8cce855212bb5746d
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Device Details

"Konica Minolta" dry laser (unsterilized)
TW: "ๆŸฏๅฐผๅก็พŽ่ƒฝ้”" ไนพๅผ้›ทๅฐ„็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

50e1f501ee8230b8cce855212bb5746d

DHA04400130405

Company Information

Product Details

Images can be recorded during diagnostic radiology.

P Radiology Science

import

Dates and Status

Oct 27, 2005

Oct 27, 2015

Aug 21, 2018

Cancellation Information

Logged out

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