29 results · 22ms · Sources: EU EUDAMED, US FDA

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LTV 1000 VENTILATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

N/A

FDA UDI
GEORGE TIEMANN & CO.·B58210517670·

ASSUFIL

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DIAMEDIX IS-CMV IGM CAPTURE TEST SYSTEM

FDA 510(k)
FDA Class 2 ·Microbiology

PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

FDA Adverse Event
MEDEL S.P.A.·Product code BTI·April 10, 2013

JAGWIRE GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·May 21, 2008

ENDOTAK SQ

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code LWS·April 12, 2011

CRANI PACK, Model/Catalog Number WECR41D, medical procedure kit.

FDA Enforcement
Class II ·Ongoing·American Contract Systems Inc·March 26, 2025

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·September 25, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·September 26, 2018

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZN·April 7, 2017

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·July 8, 2019

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·November 14, 2017

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·November 19, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·July 19, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·August 1, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·August 22, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·February 21, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·January 25, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·May 14, 2018