41 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Nihon Kohden CSM 1901 Bedside Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
LIFE SCOPE G9
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·June 13, 2024
LIFE SCOPE G9
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·October 27, 2023
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704282924·ISRAEL RETRACTOR 9 1/2" 4 PRONGS
AGC TRADITION KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304240964·
STRYKER
FDA UDI
MAKO SURGICAL CORP.·00848486029647·LID, STANDARD
AGXO
FDA UDI
Oticon A/S·05707131284402·H110V2 TI, BTE 13 WL 85 DBL AGXO
BLT Drill, long
FDA UDI
BIO CONCEPT Co., Ltd.·06947600304081·
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100257·CHU ASPIRATING SPECULUM SOLID
Malibu™
FDA UDI
Seaspine Orthopedics Corporation·10889981030094·PRECONTOURED ESS ROD, 5.5 x 80 mm
Precontoured Rod Ø5.5 mm x80 mm Package
FDA UDI
XENCO MEDICAL LLC·B064XM21510801·
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292530·Knee femur prosthesis trial - General Instrument
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292363·Knee femur prosthesis trial - General Instrument
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292240·Knee femur prosthesis trial - General Instrument
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575292868·Knee femur prosthesis trial - General Instrument
NON STICK BIPOLAR FORCEPS MODEL 07/XXX, BIPOLAR FORCEPS MODEL 08/XXX, MONOPOLAR FORCEPS MODEL 09/XXX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PHYSIOLASER OLYMPIC, SINGLE PROBES CW, CLUSTER PROBES CW, LIGHT NEEDLE, PHOTONIC SATELLITE
FDA 510(k)
FDA Class 2
·Physical Medicine
Ø5.5mm X 80mm PRECONTOURED RODS
FDA UDI
XENCO MEDICAL LLC·B064XMPH21510802·
TriVerse Femoral Trial
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215098469·
BD VACUTAINER® ECLIPSE¿ SIGNAL¿ BLOOD COLLECTION NEEDLE WITH INTEGRATED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 24, 2024