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

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VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS

FDA 510(k)
FDA Class 2 ·Cardiovascular

N/A

FDA UDI
GEORGE TIEMANN & CO.·B5821051043·HOOK, SURGICAL, GENERAL & PLASTIC SURGERY

SEMIAL 5°

FDA UDI
SIGNUS Medizintechnik GmbH·04047844000731·The KIMBA®, KIMBA® mini, MOBIS® and NOVAL™ impl...

OSMETECH MICROBIAL ANALYSER-URINARY TRACT INFECTION DETECTOR (OMA-UTI)

FDA 510(k)
FDA Class 1 ·Microbiology

KAWASUMI LABORATORY BLOOD DRAWING KIT

FDA 510(k)
FDA Class 2 ·Hematology

UNKNOWN COPELAND SHOULDER

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code HSD·April 14, 2017

COPELAND SH HUM SZ4 STND PLUS

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code HSD·June 8, 2016

UNKNOWN COPELAND HEMIARTHROPLASTY SHOULDER

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code HSD·October 21, 2016

UNKNOWN COPELAND RESURFACING SHOULDER

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code HSD·May 16, 2017

SPINEMED TABLE - FDA 510(K) K051013

FDA Adverse Event
Other ·CERT HEALTH SCIENCES, LLC·Product code ITH·July 16, 2007

UNKNOWN COPELAND SHOULDER GLENOID COMPONENT

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code HSD·July 5, 2017

SPRINT FIDELIS

FDA Adverse Event
Injury ·MPRI·Product code LWS·April 10, 2013

TENDRIL ST

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008

ENRHYTHM DR

FDA Adverse Event
Injury ·MEDTRONIC S.A.·Product code DXY·April 12, 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