16 results · 28ms · 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.

OXOID INFECTIOUS MONONUCLEOSIS KIT

FDA 510(k)
FDA Class 2 ·Immunology

Arthrex®

FDA UDI
ARTHREX, INC.·00888867047426·LO-PRO SCRW TM,SS 3.5X 40MMCORT

Oral/Enteral Syringes with ENFit connector (12 mL to 60 mL), Low Dose Tip Oral/Enteral Syringes with ENFit connector (1 mL to 6 mL)

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

A FLUOROMETER

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

GYNECARE MESH UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·June 19, 2014

BASAL/BOLUS INFUSOR 2ML X 2ML6 PACK

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 26, 2010

TOTALCARE BARIATRIC

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code FNL·November 15, 2012

LO-PRO SCRW TM,SS 3.5X 14MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019

LO-PRO SCRW TM,SS 3.5X 10MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019

LO-PRO SCRW TM,SS 3.5X 12MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019

COMPR FT SCRW,3.5 MINI,34MM LGTH

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019

LO-PRO SCRW TM,SS 3.5X 40MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019

LOCKING THIRD TUBULAR PLATE, SS, 8H

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRS·August 21, 2019

LO-PRO SCRW TM,SS 3.5X 14MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019

LO-PRO SCRW TM,SS 3.5X 40MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019

LO-PRO SCRW TM,SS 3.5X 35MMCORT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·August 21, 2019