40 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DATEX-OHMEDA COMPACT AIRWAY MODULE M-CAIOVX AND M-COVX (VERSION 01) AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Anesthesiology
Scanlan® SURG-I-BAND® color coding
FDA UDI
SCANLAN INTERNATIONAL INC·00846159001693·Scanlan® SURG-I-BAND® color coding - Labels-Pol...
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00190376004358·BATTALION, LLIF PRIMARY DISTRACTOR, 1/4" SQ. ST...
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967188393·Battalion, LLIF Trial, 0°, 18 mm Wide, 14 mm X ...
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756746571·60 In FACIO BREATHING CIRCUIT
Intervertebral Disc Preparation Instruments
FDA UDI
ALPHATEC SPINE, INC.·00190376381206·LIF, BROACH, CC OFFSET, 18MM X 14MM
Intervertebral Disc Preparation Instruments
FDA UDI
ALPHATEC SPINE, INC.·00190376380810·LIF, BROACH, STRAIGHT, 18MM X 14MM
FINGER PULSE METER
FDA 510(k)
FDA Class 2
·Cardiovascular
ELECSYS ANTI-TPO CALCHECK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197461061·TV-adapter
f=25mm...
KONG-C VBR, End Plate & Screw, 0° / 18 x 14 mm
FDA UDI
icotec AG·07640164849966·KONG-C VBR, End Plate & Screw, 0° / 18 x 14 mm
Valence Robotic Navigation System
FDA UDI
ALPHATEC SPINE, INC.·00190376647166·BROACH, LIF NAV, STRAIGHT, 18MM X 14MM
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·July 25, 2023
CABLE,ECG LEAD,OR,5L,IEC
FDA UDI
Datascope Corp.·10607567112268·CABLE,ECG LEAD,OR,5L,IEC
CABLE,ECG LEAD,OR,5L,AAMI
FDA UDI
Datascope Corp.·10607567112251·CABLE,ECG LEAD,OR,5L,AAMI
PICC NATE
FDA Adverse Event
Injury
·UTAH MEDICAL PRODUCTS, INC.·Product code LJS·January 12, 2007
PICC NATE
FDA Adverse Event
Injury
·UTAH MEDICAL PRODUCTS, INC.·Product code LJS·January 12, 2007
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·March 13, 2013
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·February 3, 2011
SOFTCLIX LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·February 19, 2008