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

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INTUITIVE SURGICAL BIPOLAR FORCEPS

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

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04047872673198·LEVAMED STABILI-TRI ANK SUP BLU R III

GC Initial™

FDA UDI
Gc America Inc.·D0470128331·Initial LiSi Press Ingot MT-D3 (3gx5)

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450311813·

EYE SENTIAL

FDA UDI
FGX INTERNATIONAL INC.·00193033444849·

AT WORK DRUG TEST, MODEL 9177T AWT

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

MODIFICATION TO STANDARD IMAGING PT 1000 ION CHAMBER

FDA 510(k)
FDA Class 2 ·Radiology

COAPTITE INJECTABLE IMPLANT

FDA Adverse Event
Other ·MERZ AESTHETICS, INC (FORMERLY BIOFORM MEDICAL, INC)·Product code LNM·October 29, 2010

DELTAPLUSH - CERECYTE MICROCOIL

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SARL·Product code HCG·June 22, 2017

ORBIT GALAXY DETACHABLE COIL SYSTEM

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017

COAPTITE INJECTABLE IMPLANT

FDA Adverse Event
Other ·MERZ AESTHETICS, INC (FORMALLY BIOFORM MEDICAL, INC)·Product code LNM·October 29, 2010

COAPTITE

FDA Adverse Event
Other ·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·March 1, 2013

ADVANTAGE SERIES 29

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FPO·March 3, 2011

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE SJ·Product code JPA·March 11, 2008

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