16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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