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"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.

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ce6e86d9d6d0b2809c93e23c915656c7
Registration Details
Taiwan FDA Registration: ce6e86d9d6d0b2809c93e23c915656c7
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Device Details

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

Registration Details

ce6e86d9d6d0b2809c93e23c915656c7

DHA04400583201

Company Information

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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