4,569 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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QC-WBS-GED
FDA UDI
CARESTREAM HEALTH, INC.·60889976571743·MOBILE STAND, 3-STEP, GED
GED (GRADUATED ELECTRONIC DECELERATOR
FDA 510(k)
FDA Class 2
·Neurology
Diacor CT Overlay
FDA UDI
Diacor, Inc.·B237GEDACS100·Coil supports for GE SIGNA PET/MR System. Inclu...
Momcozy
FDA UDI
Shenzhen Lutejiacheng Supply Chain Management Co., Ltd.·06975983271041·
95 GED DCS PLATE
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HRS·March 27, 2009
KANGAROO
FDA Adverse Event
Malfunction
·COVIDIEN·Product code LZH·June 20, 2018
OMNIPOD 5 PODS
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code QFG·January 6, 2025
NEUTROGENA MICRODERMABRASION SYSTEM
FDA Adverse Event
Injury
·JNJ CONSUMER US COSMETIC·Product code GED·December 4, 2018
BEST DERMA ROLLER TITANIUM MICRONEEDLE
FDA Adverse Event
Malfunction
·UNKNOWN·Product code GED·May 9, 2023
TITANIUM MICRONEEDLES DERMA STAMP - DERMA ROLLER ALTERNATIVE -MICRONEEDLE MICRO
FDA Adverse Event
Malfunction
·UNKNOWN·Product code GED·March 5, 2026
GLOV MICROINFUSION SYSTEM
FDA Adverse Event
Malfunction
·UNKNOWN·Product code GED·January 2, 2025
NEUROFORM EZ STENT SYSTEM
FDA Adverse Event
Injury
·STRYKER NEUROVASCULAR·Product code NJE·March 7, 2018
COBALT¿ XT HF QUAD CRT-D MRI SURESCAN¿
FDA Adverse Event
Malfunction
·MEDTRONIC EUROPE SARL·Product code NIK·August 20, 2025
SOLARA CRT-P MRI SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC EUROPE SARL·Product code NKE·March 21, 2024
HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·July 30, 2021
NIM® 3.0 MAINFRAME INTERNATIONAL
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·March 28, 2025
ET TUBE, SHER-I-BRONCH, LS, 37 FR
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CBI·July 9, 2024
ENDO CLIP
FDA Adverse Event
Malfunction
·DAVIS & GECK CARIBE LTD·Product code FZP·July 3, 2024
INCEPTIV
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·December 9, 2025
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·April 5, 2013