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

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RETIC CHEX LINEARITY

FDA 510(k)
FDA Class 2 ·Hematology

TOSCA Open end interface cable 5V FS

FDA UDI
Radiometer Basel AG·05700693096230·TOSCA Open end interface cable 5V FS

Immunalysis

FDA UDI
IMMUNALYSIS CORP·00840937108918·Multi-Drug Calibrator 2

PedCAT

FDA UDI
CURVEBEAM, LLC·00863152000300·Cone Beam Computed Tomography diagnostic imagin...

RECLAIM

FDA UDI
DEPUY (IRELAND)·10603295543879·RECLAIM MONOBLOC REVISION HIP SYSTEM MONOBLOC ...

Mariner Outrigger

FDA UDI
Seaspine Orthopedics Corporation·10889981172671·Axial, Closed, 115mm

Golden Isles Pedicle Screw System

FDA UDI
Intelivation, LLC·G079C2530001150·Curved Anti-Rotation Ti Rod, 115mm

e-vive NMES System; 2XL/3XL, Right

FDA UDI
Motive Health, Inc.·00854816006899·e-vive NMES System; 2XL/3XL, Right

PedFlex Flexible Nailing System

FDA UDI
ORTHOPEDIATRICS CORP.·00841132119419·ø1.5mm Flexible IM Nail Cap (2 Each)

Golden Isles Pedicle Screw System

FDA UDI
Intelivation, LLC·G079C2520001150·Curved Ti Rod, 115mm

Taurus Pedicle Screw System

FDA UDI
SINTX Technologies, Inc.·M555500000115·Taurus Implant Caddy- Screws

BARCOMED 2MP2

FDA 510(k)
FDA Class 2 ·Radiology

MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),

FDA 510(k)
FDA Class 2 ·Neurology

EQ-5000 EQUATOR CONVECTIVE WARMER

FDA Adverse Event
Injury ·SMITHS MEDICAL ASD, INC.·Product code DWJ·September 21, 2009

PedFlex Flexible Nailing System

FDA UDI
ORTHOPEDIATRICS CORP.·00840194418287·Ø1.5 MM FLEXIBLE IM NAIL CAP (2 EACH)

RS GLENOID PLATE EXT CAG +10MM CAGE PEG

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWS·July 17, 2023

EQUINOXE REVERSE 42MM HUMERAL LINER +2.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·August 7, 2023

MEGASUTURECUT NEEDLEDRIVER INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·March 8, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011

SYNCHROMED EL

FDA Adverse Event
Injury ·RICE CREEK MANUFACTURING·Product code LKK·February 19, 2008