18 results · 21ms · Sources: EU EUDAMED, US FDA

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72 DETERM. SIZE RADIAL IMMUNO. TEST HUMAN CERULOPL

FDA 510(k)
FDA Class 2 ·Immunology

NAR Kit

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209102372·KIT, IPOK - COMBAT GAUZE w' HYFIN

LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1)

FDA 510(k)
FDA Class 1 ·Clinical Toxicology

CUSA Excel+

FDA 510(k)
FDA Unclassified ·Unknown

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 30, 2026

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 21, 2014

LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

FDA Adverse Event
Injury ·ALLERGAN·Product code LTI·November 20, 2012

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code MDS·October 1, 2010

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

NEXIVA DIFFUSICS

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 16, 2026

Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

FDA Enforcement
Class II ·Terminated·STERILMED, INC.·December 16, 2015