16 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MG ATC: ATTENUATION CORRECTION SYSTEM FOR DUAL-HEAD VARIABLE-ANGLE GAMMA CAMERA
FDA 510(k)
FDA Class 2
·Radiology
NA
FDA UDI
Synthes GmbH·10886982202505·SMALL HOHMANN RETRACTOR 6MM SHORT NARROW TIP 160MM
Belimed Steam Sterilizer MST-H TOP 5000
FDA 510(k)
FDA Class 2
·General Hospital
CENTRIA PHENYTOIN RIA TEST SET
FDA 510(k)
FDA Class 2
·Clinical Toxicology
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·March 6, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 30, 2025
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·November 24, 2025
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 15, 2025
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 9, 2025
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 4, 2025
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 24, 2025
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·January 12, 2026
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·March 4, 2026
PCCO MONITORING KIT
FDA Adverse Event
Malfunction
·PULSION MEDICAL SYSTEMS SE·Product code KRB·February 19, 2026