15 results · 24ms · Sources: EU EUDAMED, US FDA

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INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODEL IS1000

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

2040 Ceramic Brackets

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746005473·COSMETIC 20/40 LL 2ND BIC 022 T-22 A=0 R=0

RD-3008

FDA 510(k)
FDA Class 2 ·Dental

SENSITITRE 18-24 HOURS SUSCEPTIBILITY PLATES (MOXIFLOXACIN)

FDA 510(k)
FDA Class 2 ·Microbiology

MODIFIED KUGEL PATCH

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·October 7, 2010

MODIFIED KUGEL PATCH

FDA Adverse Event
Malfunction ·DAVOL INC.·Product code FTL·September 1, 2011

VASONOVA VPS BEDSIDE KIT

FDA Adverse Event
Malfunction ·VASONOVA·Product code OBJ·March 20, 2013

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011

30" TRANSPORT STRETCHER

FDA Adverse Event
Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPO·March 28, 2008

MODIFIED KUGEL PATCH

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·June 27, 2013

MODIFIED KUGEL PATCH

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·May 25, 2016

MODIFIED KUGEL PATCH

FDA Adverse Event
Injury ·DAVOL INC·Product code FTL·August 2, 2011

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

Ellipse Implantable Cardioverter Defibrillators (ICDs), Model No. CD1275, CD1311, CD2275, CD2311, CD1411, CD2411 Ellipse ST Implantable Cardioverter Defibrillators (ICDs), Model No. CD1273, CD1309, CD1409, CD2273, CD2309, CD2409.

FDA Enforcement
Class II ·Terminated·St Jude Medical Cardiac Rhythm Management Division·September 10, 2014