43 results · 23ms · Sources: EU EUDAMED, US FDA

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URISITE URINE COLLECTION KIT FOR MICROALBUMIN/CREATININE TESTING

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

3i Certain

FDA UDI
Preat Corporation·00842092167229·Biomet 3i Certain®-compatible 5.0mm Engaging Pl...

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040015667·Retractor Senn Blunt

Scanlan® SURG-I-BAND® color coding

FDA UDI
SCANLAN INTERNATIONAL INC·00846159001655·Scanlan® SURG-I-BAND® color coding - Labels-Sol...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450139417·

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00190376004310·BATTALION, LLIF PRIMARY DISTRACTOR, 1/4" SQ. ST...

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00840967188355·Battalion, LLIF Trial, 0°, 18 mm Wide, 10 mm X ...

CARDIOSAVE

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·September 3, 2014

QUALITROL LIPID CONTROL, LEVELS 1 AND 2

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

ASCENT KNEE REVISION FEMORAL STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 19, 2023

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00811801038709·Battalion, LLIF Broach, Straight, 18mm x 10mm

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00811801036811·18x45 Distractor Rasp – 10mm, Offset

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00811801036347·18x45 Distractor Rasp – 10mm

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00840180501375·18x45 Distractor Rasp – 10mm

Intervertebral Disc Preparation Instruments

FDA UDI
ALPHATEC SPINE, INC.·00190376380773·LIF, BROACH, STRAIGHT, 18MM X 10MM

Intervertebral Disc Preparation Instruments

FDA UDI
ALPHATEC SPINE, INC.·00190376381169·LIF, BROACH, CC OFFSET, 18MM X 10MM

SE-001810 / KW-056-004 / Disposable electrode pads 55x55mm

Device
EU MDR · Eu Md Class 1 ·Shenzhen Keborui Electronics Co., Ltd·On the market

Valence Robotic Navigation System

FDA UDI
ALPHATEC SPINE, INC.·00190376647128·BROACH, LIF NAV, STRAIGHT, 18MM X 10MM

INFINION? PRO

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 2, 2025