8 results
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18ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FUKUDA DENSHI: CARDIOMAX, MODEL FX-4010 MULTI CHANNEL ELECTROCARDIOGRAPH
FDA 510(k)Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981066·anteriors; shade A3; mould BIM2
Adler Instrument Company
FDA UDI
Adler, Inc.·00810123209637·Freeman Rake Retractor 4 prong, sharp OL 185mm ...
Powder Free Nitrile Examination Glove (Blue) with Low Dermatitis claim and with tested for Use with Chemotherapy Drugs Claims
FDA 510(k)
FDA Class 1
·General Hospital
BRACHYTHERAPY SOURCE DEVICE, MODEL 9011
FDA 510(k)
FDA Class 2
·Radiology
DEXTRUS 4136
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code DTB·February 19, 2013
PRATT RECTAL PROBE 73/4 SILVER
FDA Adverse Event
Malfunction
·Product code ITX·November 22, 2010
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 24, 2014