11 results
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26ms
·
Sources: EU EUDAMED, US FDA
NON CONDUCTIVE PEDIATRIC ANES. FACE
FDA 510(k)
FDA Class 1
·Anesthesiology
Traverse
FDA UDI
Nuvasive, Inc.·00887517153456·Traverse Plate, Size 45 Compression
PreView™
FDA UDI
NEXUS SPINE, L.L.C.·B6788210450·Locking Punch Rod - Cervical
Tube Lock Small Females (4)
FDA UDI
STERNGOLD DENTAL LLC·00841549116476·Used by the laboratory as a pattern (male and f...
LOQTEQ®
FDA UDI
aap Implantate AG·04042409346033·LOQTEQ Screw guide sleeve 4.5, blue
ERA IMPLANT
FDA 510(k)
FDA Class 2
·Dental
HUMAN ALBUMIN CSF KIT
FDA 510(k)
FDA Class 2
·Immunology
FOLFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 20, 2014
CUSTOM PAK
FDA Adverse Event
Injury
·ALCON - HOUSTON·Product code KYG·October 25, 2012
CELL-DYN 1800 ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·August 31, 2010
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