14 results · 21ms · Sources: EU EUDAMED, US FDA

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ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

FDA Adverse Event
Malfunction ·AESCULAP AP & CO. KG·Product code GEI·March 27, 2015

CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

CAIMAN DISP.INSR.ARTICULAT.D:12 / 240MM

FDA Adverse Event
Malfunction ·AESCULAP AG& CO. KG·Product code GEI·April 15, 2015

CAIMAN DISP INSTR ARTICULAT D:12/240MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 16, 2014

CAIMAN DISP. INSTR. ARTICULAT. D.: 12/440MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·July 28, 2014

KNIGHTSTAR 330 VENTILATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE

FDA 510(k)
FDA Class 2 ·Microbiology

PEN NDL 31GA 5MM 100BX 1200 USA

FDA Adverse Event
Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·April 17, 2025

INVIVO CORPORATION EXPRESSION MRI PATIENT MONITORING SYSTEM

FDA Adverse Event
Malfunction ·INVIVO CORPORATION·Product code MWI·April 14, 2011

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 3, 2013

ALARIS LVP (8100)

FDA Adverse Event
Injury ·CARFUSION·Product code FRN·September 10, 2014

145-DEG PE 36MM HUM LINER +0

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWS·December 10, 2024

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012