60 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Quantum PureFlow Standard Heat Exchanger and Quantum PureFlow Cardioplegia Heat Exchanger
FDA 510(k)
FDA Class 2
·Cardiovascular
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112793·BARRON VACUUM PUNCH 8.5MM
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR32201101·Fixation element for slider
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113003·PS Insert, Size 1 x 10mm
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220110150·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220110070·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220110000·
TALOS®-TL
FDA UDI
SpineArt SA·07640375239105·TALOS®-TL (HA) PEEK IBFD L22 W09 H10
ELEGANT NITRILE POWDER FREE EXAMINATION GLOVE BLUE VIOLET
FDA 510(k)
FDA Class 1
·General Hospital
MODIFICATION TO TRELEX MESH SURGICAL MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GS
FDA Adverse Event
Malfunction
·LEONHARD LANG GMBH·Product code MKJ·November 25, 2022
ONE TOUCH BASIC ENHANCED
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·August 12, 2002
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 3, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025
TERUMO C121 (HF/CR 1.2L)
FDA Adverse Event
Other
·TERUMO·Product code FJI·December 21, 1994
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 30, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 13, 2017
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 21, 2024