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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

ULTRA SEAL STERILE LUBRICATING JELLY

FDA 510(k)
FDA Class 1 ·General Hospital

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526189713·LEVAMED ACTIVE ANKLE SUP BLACK L II

Medline Industries, Inc.

FDA UDI
MEDLINE INDUSTRIES, INC.·10198459034565·CENTRAL LINE SET

Portex

FDA UDI
ICU MEDICAL, INC.·00351688002504·

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383501477·Gutta Percha Points is used to root canal filin...

ALLURE® MB

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807101522041·ALLURE® MB SEW .022 UPPER 2

TRANSQ3

FDA 510(k)
FDA Class 2 ·Physical Medicine

RESORBABLE BONE PINS

FDA 510(k)
FDA Class 2 ·Orthopedic

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 9, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 1, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·June 8, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·April 26, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·April 20, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

WAVEWRITER ALPHA

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 29, 2022

BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 21, 2019

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 2, 2013

UNIVERSAL FEM SLV FUL POR 46MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·September 19, 2014

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·May 20, 2011