29 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT
FDA 510(k)
FDA Class 1
·Microbiology
Bard® Blakemore Esophageal-Nasogastric Tube
FDA UDI
C. R. Bard, Inc.·00801741076831·Bard® Blakemore Esophageal-Nasogastric Tube
Young
FDA UDI
YOUNG DENTAL MANUFACTURING I, LLC·00302730923001·Young Standard Prophy Brush, Firm, Long Flat Bl...
Zavation
FDA UDI
Zavation LLC·00842166126473·eZspand PLIF/T-PLIF 9x23x0°, 10.5-15mm
Victoria Klein
FDA UDI
Diversified Products, Inc.·00037741909286·
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702429374·ELVAREX 1/THIGH HIGH/SLANT-OPEN TOE/DOTTED 2,5 ...
AMC
FDA UDI
Advantage Medical Electronics, LLC·00849593020978·12' Philips Temp Adapter Cable w/2 pin DIN
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702357899·Elvarex 2/Knee High/Open Toe-Elephantiasis-Vers...
Cosmolock
FDA UDI
Kalitec Direct LLC·B07310K0123000·Recovery Tube, MIS
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094032970·PROPAQ LT CHARGING CRADLE PLUG TYPE C
SUPER 6
FDA 510(k)
FDA Class 2
·Dental
ACON BZO ONE STEP BENZODIAZEPINES TEST STRIP; ACON BZO ONE STEP BENZODIAZEPINES TEST DEVICE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
BARD® BLAKEMORE ESOPHAGEAL-NASOGASTRIC TUBE
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code KNT·January 23, 2026
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 18, 2025
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·July 2, 2019
BARD® BLAKEMORE ESOPHAGEAL-NASOGASTRIC TUBE
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code KNT·January 13, 2026
Bard Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code KNT·April 17, 2025
STEALTHSTATION S7 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·May 3, 2013
CRYSTALENS ACCOMODATING IOL
FDA Adverse Event
Injury
·Product code NAA·August 20, 2014
GO BED II MED/SURG MED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 3, 2011