25 results · 20ms · Sources: EU EUDAMED, US FDA

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NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL CANNULA MANUFACTURED BY HRCI

FDA 510(k)
FDA Class 1 ·Anesthesiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526189744·LEVAMED ACTIVE ANKLE SUP BLACK L V

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526780774·LEVAMED ACTIVE ANKLE SUP SLVR L V

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040013939·Zirlux 16+ D4 98.5X18

2011 125

Device
EU MDR · Eu Md Class 1 ·VOE , S.A·On the market

NA

FDA UDI
Stryker GmbH·00886385005034·High Strength T7 Driver

Cosmolock

FDA UDI
Kalitec Direct LLC·B07311K0112250·Tap, 7.50mm, Cannulated, Fixed Sleeve

RADIESSE DERMAL FILLER

FDA Adverse Event
Injury ·BIOFORM MEDICAL, INC.·Product code LMH·November 24, 2008

INSTANT-VIEW BARBITUATE URINE DIP STRIP TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING

FDA 510(k)
FDA Class 1 ·Ophthalmic

PRECISION MONTAGE MRI

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 23, 2021

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197038003·Super-Cut Waldram Handsurgery Scissors curved...

OneLIF™

FDA UDI
Novapproach Spine LLC·G07001112516060·Trial-OneLIF Interbody, Small, 25 Degree, 16mm ...

OneLIF™

FDA UDI
Novapproach Spine LLC·G07001112518080·Trial-OneLIF Interbody, Small, 25 Degree, 18mm ...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197417273·Graefe Skin Hook blunt,...

GMK-SPHERE 02.12.0410FL TIBIAL INSERT FIXED SPHERE FLEX SIZE 4/10 MM L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 6, 2022

GMK SPHERE TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 25, 2025

K-wire, double trocar 1.1/125mm

FDA UDI
mahe medical gmbh·EMAH00406000111250·K-wire, double trocar 1.1/125mm

VIBRANT SOUNDBRIDGE

FDA Adverse Event
Injury ·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·March 15, 2013

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEATHCARE·Product code KDJ·March 8, 2011