30 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MULTI FRAME WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958001468·600 Micron Disposable Diode Laser Lightguide, 3...
CEDIA Barbiturate Assay
FDA UDI
Microgenics Corporation·00884883001411·
TruLock
FDA UDI
Rmo, Inc.·00885797648013·TRULOCK Primer Activated Adhesive Mini Kit (1ea...
Merit® Kit
FDA UDI
Merit Medical Systems, Inc.·00884450478912·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450171547·
GEN4 Direct Access
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828134798·GEN4 Direct Access
Ball Abutment Transfer (2 pieces)
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307121015·
Ball Abutment Transfer
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307129868·
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494460838·Trephine Protection Tube
ID 5.2mm, OD 6.0mm, WL...
Calcshift Instrument System
FDA UDI
Medartis Inc.·00810082898293·CalcShift Positioning Frame Rail Screw
REAL PATIENT REAL PATIENT 128 CHANNEL EEG HEADBOX, MODEL EX-NW-128-RP
FDA 510(k)
FDA Class 2
·Neurology
ENRAF-NONIUS SONOPULS 190 SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
BodyForm™ Thoraco-Lumbar
FDA UDI
Seaspine Orthopedics Corporation·10889981048235·Thoraco-Lumbar 84mm Plate (BFP-42-0-C)
8-CHANNEL ADAPTER, BSX, 10CM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·November 7, 2023
PAINSMART
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·April 29, 2013
AUTOSONIX ULTRA SHEARS 5MM INSTRUMENT
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL·Product code LFL·May 16, 2011
PROXIMATE RELOADABLE LINEAR STAPLER - 30 MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code GDW·August 5, 2008
MCLEAN-RING NASOJEJUNAL FEEDING TUBE SET
FDA Adverse Event
Injury
·COOK INC·Product code KNT·November 10, 2021
SMR CEMENTLESS FINNED STEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code HSD·July 29, 2021