12 results
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19ms
·
Sources: EU EUDAMED, US FDA
STAGE ZERO AIR FLOTATION BED
FDA 510(k)
FDA Class 2
·Physical Medicine
Surgimedics®
FDA UDI
COASTAL LIFE TECHNOLOGIES, INC.·00814716020661·Smoke Evacuation Tubing
Symmetry Surgical
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482129869·Symmetry® Probe; Palpitation; 12 5/8 in; 32 cm
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·00842331120497·PALPATATION PROBE, 5.0mm
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776083984·Palpation Probe
CONSTANT CURRENT STIMULATOR MODEL 022101
FDA 510(k)
FDA Class 2
·Cardiovascular
KESTREL LENS CASE 731H-893S/P-1700-2611
FDA 510(k)
FDA Class 2
·Ophthalmic
SOFT-VU ANGIOGRAPHIC CATHETER
FDA Adverse Event
Malfunction
·ANGIODYNAMICS, INC.·Product code DQO·June 10, 2014
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·November 22, 2010
TENDRIL STS
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 9, 2013
smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·March 27, 2024
paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·October 2, 2024