22 results
·
20ms
·
Sources: EU EUDAMED, US FDA
DATA RECORDER
FDA 510(k)
FDA Class 2
·General Hospital
Vivid KleenSert
FDA UDI
PEARSON DENTAL SUPPLIES, INC.·D724R9101180·IF-10 25k
CoRoent
FDA UDI
Nuvasive, Inc.·00887517389756·CoRoent XL Tray, XLIF Instruments
8 Degree Lordotic, Opticage Expandable Interbody Implant
FDA UDI
INTERVENTIONAL SPINE, INC·00811954013417·18mm Width x 50mm Length by 11mm-16mm Footprint...
UCR
FDA UDI
Seaspine Orthopedics Corporation·10889981079642·Install / Remove Tool, 8.0
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375008782·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009284·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009246·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009253·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009314·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375000502·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009260·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009307·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009291·NA
Orascoptic - Spark Headlight System
FDA UDI
METREX RESEARCH, LLC·00615375009277·NA
MaxCare 8910-118 205*118*17cm
Device
EU MDR
·
Eu Md Class 1
·Vevia Finland Oy·On the market
NORMED MANDIBULAR FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
STIMTRODE SINGLE USE NERVE STIMULATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
ROTALINK? PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code MCX·July 2, 2014
SERVO-I
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·November 9, 2012