48 results
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61ms
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Sources: EU EUDAMED, US FDA
Compact Medical Inc.
FDA registration
Compact Medical Inc.·1 product·🇺🇸 United States
butterflyBVM
FDA UDI
Compact Medical Inc.·00860012073535·
butterflyBVM READY
FDA UDI
Compact Medical Inc.·00860012073528·
butterflyBVM, READY
FDA UDI
Compact Medical Inc.·00860012073573·
butterflyBVM
FDA UDI
Compact Medical Inc.·00860012073504·
butterflyBVM PLUS
FDA UDI
Compact Medical Inc.·00860012073511·
butterflyBVM, PLUS
FDA UDI
Compact Medical Inc.·00860012073559·
Sovereign¿ Compact Phacoemulsification System, v 5.3, Part Number: CMP680300. The system is used for cataract surgery.
FDA Enforcement
Class II
·Terminated·Abbott Medical Optics, Inc.·July 17, 2013
UNKNOWN NASOGASTRIC TUBE
FDA Adverse Event
Malfunction
·AVANOS MEDICAL INC.·Product code KNT·February 9, 2026
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 29, 2010
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 31, 2010
Sovereign Compact Phacoemulsification System, v 5.3, Part Number: CMP680300. The system is used for cataract surgery.
FDA Recall
Terminated
·Abbott Medical Optics, Inc.·Product code HQC·May 23, 2013
DISPOSABLE 20GA VITRECTOMY CUTTER & IRRI
FDA Adverse Event
Injury
·MEDICAL INSTRUMENT DEVELOPMENT LABS INC (MIDLABS)·Product code MLZ·June 23, 2022
Medtronic 3778 Lead Kit, 1x8 Compact Low Impedance Lead Kit for Spinal Cord Stimulation (SCS). Manufactured at: Medtronic, Inc., Villalba, Puerto Rico USA. Medtronic, Inc., Minneapolis, MN 55432-5604.
FDA Recall
Terminated
·Medtronic Neurological·Product code LGW·August 2, 2006
MOBILE FLUOROSCOPIC IMAGE INTENSIFIED SYSTEM
FDA Adverse Event
Malfunction
·OEC MEDICAL SYSTEMS, INC.·Product code JAA·March 17, 1998
FREESTYLE COMFORT
FDA Adverse Event
Malfunction
·CAIRE INC.·Product code CAW·September 1, 2022
STA COMPACT
FDA Adverse Event
DIAGNOSTICA STAGO, GENNEVILLIERS·Product code GKP·June 16, 2014
Spacelabs qube Compact Monitor, Model 91390. The monitor is functioning as either bedside or central monitors; passively displays data generated by Spacelabs Healthcare parameter modules, Flexports interfaces, and other SDLC based products in the form of waveform and numeric displays, trends and alarms.
FDA Recall
Terminated
·Spacelabs Healthcare Inc·Product code MHX·May 8, 2015
Medtronic 3777 Lead Kit, 1x8 Low Impedance Lead Kit for Spinal Cord Stimulation (SCS). Manufactured at: Medtronic, Inc., Villalba, Puerto Rico USA. Medtronic, Inc., Minneapolis, MN 55432-5604.
FDA Recall
Terminated
·Medtronic Neurological·Product code LGW·August 2, 2006
DISPOSABLE 20GA VITRECTOMY CUTTER & IRRI
FDA Adverse Event
Injury
·MEDICAL INSTRUMENT DEVELOPMENT LABS INC (MIDLABS)·Product code MLZ·June 23, 2022