Taiwan FDA registration 50e1f501ee8230b8cce855212bb5746d

"Konica Minolta" dry laser (unsterilized)

TW: "柯尼卡美能達" 乾式雷射片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·KONICA MINOLTA MEDICAL & GRAPHIC, INC.·Registered Oct 27, 2005 – Oct 27, 2015Cancelled
Registration details
Analysis ID
50e1f501ee8230b8cce855212bb5746d
Customs Code
DHA04400130405
Company information
Manufacturer Country
Japan
Authorized Representative
MEDEPOCH TRADING CO., LTD.
Product details
Intended Use
Images can be recorded during diagnostic radiology.
Product Type (Level 1)
P Radiology Science
Import Information
import
Dates and status
Registration Date
Oct 27, 2005
Expiry Date
Oct 27, 2015
Cancellation Date
Aug 21, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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