30 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TIARA MEDICAL SYSTEMS ADVANTAGE II NASAL MASK, MODELS TMS-2520 AND TMS-2530
FDA 510(k)
FDA Class 2
·Anesthesiology
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR20319351·BioStarter wires Euro-Smile-F. mand. .014"
ACCESS TESTOSTERONE REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33560, 33565
FDA 510(k)
FDA Class 1
·Clinical Chemistry
REJUVENIQUE MODEL #RJV10
FDA 510(k)
FDA Class 2
·Neurology
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 10, 2019
VC10 PUMP, 115V
FDA Adverse Event
Malfunction
·GYRUS ACMI, INC.·Product code HHK·January 2, 2025
DEROYAL
FDA Adverse Event
Other
·DEROYAL GUATEMALA·Product code LGF·March 26, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 28, 2011
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code LDD·April 18, 2008
METASUL, ALPHA INSERT, II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·March 15, 2018
METASUL, ALPHA INSERT, II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·June 25, 2018
DURASUL, ALPHA INSERT, KK/36
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LZO·March 6, 2018
DURASUL, ALPHA INSERT, HOODED, MM/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·May 22, 2018
DURASUL, ALPHA INSERT, HH/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LZO·June 4, 2018
DURASUL, ALPHA INSERT, HOODED, LL/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code JWH·April 23, 2018
METASUL, ALPHA INSERT, JJ/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·April 16, 2018
COCR HEAD 28/-4 'S' 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·May 22, 2018
DURAL ALPHA INSERT NEUTR LL/36
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·May 9, 2019
METASUL, ALPHA INSERT, JJ/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·August 7, 2018
METASUL ALPHA INSERT, JJ/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·August 3, 2018