14 results · 19ms · Sources: EU EUDAMED, US FDA

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MASEP SRRS GAMMA RAYS STEREOTACTIC RADIATION THERAPY SYSTEM FOR HEADS (MASEP GAMMA THERAPY SYSTEM)

FDA 510(k)
FDA Class 2 ·Radiology

Flex

FDA UDI
Diversified Products, Inc.·00037741504115·

Arthrex®

FDA UDI
ARTHREX, INC.·00888867522497·Cannulated Canc Screw,36mm Thd,7.0x125mm

AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 125mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010114·

Flex

FDA UDI
Diversified Products, Inc.·00842894114742·

NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL CANNULA MANUFACTURED BY HRCI

FDA 510(k)
FDA Class 1 ·Anesthesiology

GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING

FDA 510(k)
FDA Class 1 ·Ophthalmic

FENESTRATED BIPOLAR FORCEPSINSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 4, 2013

INSIGNIA

FDA Adverse Event
Malfunction ·GUIDANT CLONMEL IRELAND·Product code NVZ·April 8, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011

XIA LP POLYAXIAL SCREW 5.5 X 45MM

FDA Adverse Event
Injury ·STRYKER SPINE BORDEUX·Product code HWC·May 6, 2008

BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 100 MG/20 MG

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·December 28, 2018

BD VACUTAINER® BLOOD ALCOHOL DETERMINATIONS SODIUM FLUORIDE: POTASSIUM OXALATE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·June 25, 2019

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