26 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SIEMENS INFINITY SC 6002XL ENHANCED WITH ST SEGMENT ANALYSIS
FDA 510(k)
FDA Class 2
·Cardiovascular
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950018451·FORCEP TISSUE GERALD 1X2 TEETH CURVED 7" 18CM
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00271051·
artVeneer life
FDA UDI
Merz Dental GmbH·D7092002105·artVeneer life lower posteriors, M, C2
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112748·BARRON VACUUM PUNCH 7.25MM
ISCOVE'S MODIFIED DELBECCO'S MEDIUM NO.200-2105
FDA 510(k)
FDA Class 1
·Hematology
MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),
FDA 510(k)
FDA Class 2
·Neurology
MOSS MIAMI 6.35MM ROD SYSTEM PEDICLE AND LAMINAR HOOKS
FDA 510(k)
FDA Class 2
·Orthopedic
NEEDLE 18X1-1/2 BLUNT FILL
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code GAA·July 3, 2025
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 13, 2022
VENTED MICRO VOL.INLET, N/S
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·March 28, 2022
VALVE SET, EM2400
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·April 7, 2022
VALVE SET, EM2400
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·August 8, 2022
LUMAX 540 HF-T
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NIK·March 13, 2013
ACCU-CHEK CARTRIDGE
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·February 4, 2011
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 20, 2008
250 ML TPN BAG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 21, 2021
EXACTA-MIX 2400 COMPOUNDING SYSTEM
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code NEP·February 27, 2023
TPRLC 133 MP TYPE1 PPS SO 17.0 1
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KWA·November 7, 2019
TPRLC XR MP FP T1 PPS 6X97.5MM MM T1
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·November 7, 2019