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

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M3 (MICRO-MULTILEAF COLLIMATOR)

FDA 510(k)
FDA Class 2 ·Radiology

Safco NiTi RL Rotary Files

FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310208603·Safco NiTi RL rotary files, #30, (0.6 taper / 2...

APC™ PLUS Unitek™ Mini Uni-Twin

FDA UDI
3M UNITEK CORPORATION·00652221094032·Mini Uni-Twin(TM) Bracket APC(TM) PLUS LR4 -17T...

APC™ II Unitek™ Mini Uni-Twin

FDA UDI
3M UNITEK CORPORATION·00652221063014·Mini Uni-Twin(TM) Bracket APC(TM) II LR4 -17T/0...

FUTURA SAFETY SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

MODEL 6900GE-64: C-SPINE ARRAY

FDA 510(k)
FDA Class 2 ·Radiology

BIO-COMP INTERFSCRW W/DISP SHTH

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MAI·March 27, 2019

BIO-COMP INTERFSCRW W/DISP SHTH

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MAI·March 27, 2019

BIO-COMP SWVLKC CLD 4.75X19.1MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MAI·March 27, 2019

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC.·Product code LFR·May 30, 2007

EMAX 2 PLUS MOTOR

FDA Adverse Event
Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·March 18, 2013

FLAIR

FDA Adverse Event
Injury ·BARD PERIPHERAL VASCULAR·Product code MIH·August 1, 2014

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

The Propaq LT Series monitors. Model numbers 802LTAN, 802LT0N, and 802LTRN. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medical-surgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. intended to be used by clinicians and medically qualified personnel for single or multiparameter vital signs monitoring of ambulatory and nonambulatory patients, including neonate, pediatric and adult patients. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medicalsurgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. The monitors can be used as stand-alone devices or as devices networked to an Acuity Central Station through wireless communication over a Welch Allyn FlexNet network.

FDA Enforcement
Class II ·Terminated·Welch Allyn Protocol, Inc·January 15, 2014