3,718 results · 84ms · Sources: EU EUDAMED, 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