32 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SUNMED GUIDE WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
NOVO Health Services, LLC
FDA UDI
NOVO HEALTH SERVICES, LLC·00812564031433·Set Up Pack, Standard
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319739426·Adson Dressing Forceps 4-3/4" (11.9cm), serrate...
PMT® CORPORATION HALO
FDA UDI
PMT CORPORATION·10650551093128·CHEST BLOCK ASSEMBLY
ADULT DUAL-HEATED EVAQUA BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZE·August 13, 2012
VECTORSONIC, MODEL VU-200
FDA 510(k)
FDA Class 2
·Physical Medicine
SUR-G GLOV AND MAXITEX
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
KING SEPTEMS
FDA Adverse Event
Malfunction
·KING SEPTEMS·Product code LMA·November 1, 2012
Widex
FDA UDI
Widex A/S·05706069923247·WIDEX MOMENT MBB3D 220 (Silver grey)
Widex
FDA UDI
Widex A/S·05706069884333·WIDEX MOMENT MRR2D (Silver Grey ) 220, RC coil,...
Widex
FDA UDI
Widex A/S·05706069794441·Widex EVOKE E-FP (Silver Grey ) 220, Telecoil, ...
Widex
FDA UDI
Widex A/S·05706069972047·WIDEX MOMENT MBB2 220 (Silver grey)
Widex
FDA UDI
Widex A/S·05706069806311·Widex EVOKE E-FA (Silver Grey ) 220, Telecoil, ...
Widex
FDA UDI
Widex A/S·05706069807356·Widex EVOKE E-FM (Silver Grey ) 220, RC coil
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 2, 2015
ADULT INSPIRATORY-HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·May 21, 2012
STOCKERT 70 RF GENERATOR
FDA Adverse Event
Injury
·STOCKERT GMBH·Product code DRF·April 24, 2013
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·May 15, 2009
Bone Marrow Biopsy Tray Catalog Number: 8917R1
FDA Enforcement
Class II
·Terminated·Busse Hospital Disposables, Inc.·June 8, 2022
LIGACLIP** ENDOSCOPIC CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·May 20, 2013