26 results
·
22ms
·
Sources: EU EUDAMED, US FDA
SIMPLY SLICK PERSONAL LUBRICATING LOTION
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699564·GENUMEDI PSS BLUE, SIZE IV
CoRoent
FDA UDI
Nuvasive, Inc.·00887517565686·CoRoent Ant TLIF PEEK, 14x10x30mm 4°
PRINCETON
FDA UDI
Princeton Medical Group, Inc.·00810158217201·FORCEPS JEWELER FIG. 3C .5MM TIP 4.25"
ADSON TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896023482·ADSON TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLAT...
PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50
FDA 510(k)
FDA Class 2
·Cardiovascular
ST AIA PACK HBA1C
FDA 510(k)
FDA Class 2
·Hematology
HIGH FREQUENCY VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·December 4, 2014
LOGIC FEMORAL PS POR RIGHT SZ 2
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 10, 2025
GMK PS FEMUR CEMENTED SIZE 2 LEFT
FDA Adverse Event
MEDACTA INTL SA·Product code JWH·May 24, 2013
EEA 28MM SINGLE-USE STAPLER
FDA Adverse Event
Injury
·USSC PUERTO RICO·Product code GDW·June 15, 2011
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·October 3, 2014
LOGIC CR FEMORAL POR, LEFT, SZ 3.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 11, 2024
ALARIS SYSTEM
FDA Adverse Event
Injury
·CAREFUSION SD·Product code FRN·May 13, 2022
ALARIS SYRINGE PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·December 23, 2020
VACUTAINER ULTRATOUCH
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code FPA·March 23, 2026
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 29, 2022
CATHETER MOUNT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BZO·December 29, 2014
INFANT DUAL HEATED EVAQUA2 BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·December 4, 2014
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 26, 2023