3,718 results
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84ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·10017344000075·Drionic Underarm Device Pair
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000061·Drionic Hand/Foot Device
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000122·Drionic Underarm Large Parts Kit
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000009·Drionic Underarm Applicator Modules
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000023·Drionic Underarm Pads
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000078·Drionic Underarm Device
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000054·Drionic Alkaline Battery
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000115·Drionic Hand/Foot Large Parts Kit
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000092·Drionic Underarm Parts Kit
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000085·Drionic Alkaline Battery Pair
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000030·Drionic Hand/Foot Plates
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000016·Drionic Hand/Foot Pads
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000108·Drionic Hand/Foot Parts Kit
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·00017344000047·Drionic Underarm Shoulder Straps
Drionic TM
FDA UDI
GENERAL MEDICAL COMPANY·10017344000068·Drionic Hand/Foot Device Pair
SIGNA HORIZON LX SHORT BORE SR77 1.5T
FDA Adverse Event
Other
·GE MEDICAL SYSTEMS, GENERAL ELECTRIC COMPANY·Product code LNH·April 29, 2003
GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece Neonatal Patient Circuit Kit Disposable with Size 1 Mask***M1091335 QTY: 10 T-Piece Disposable Circuit, QTY: 10, M1091316 T-Piece Disposable Circuit Kit with Mask Size O; M1091365 QTY: 10 T-Piece Disposable Circuit Kit with Mask, Size 1, Lot 1981713 *** Ohmeda Medical, A Division of Datex-Ohmeda, Inc. A General Electric Company Laurel, MD 20723 USA MADE IN USA*** Provides the basic equipment required for pulmonary resuscitation of infants.
FDA Enforcement
Class I
·Terminated·GE Healthcare, LLC·January 2, 2013
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·October 25, 2018
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006