19 results · 31ms · 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.

TOTAL WORK INTEGRATOR, MODEL #940-110

FDA 510(k)
FDA Class 2 ·Physical Medicine

EMT - Siemens Trauma - Red Bag

FDA UDI
Certified Safety Manufacturing, Inc.·00766588226033·EMT - Siemens Trauma - Red Bag

IMMULITE 1000 AUTOMATED IMMUNOASSAY ANALYZER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ONTEX AND OTHER PROPRIETARY NAMES

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

AUTOSOFT XC

FDA Adverse Event
Injury ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

AUTOSOFT XC

FDA Adverse Event
Injury ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

AUTOSOFT XC

FDA Adverse Event
Injury ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

AUTOSOFT XC

FDA Adverse Event
Injury ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

OXFORD PKS ANATOMIC ARCOM MENISCAL BEARING MEDIUM LEFT SIZE 3

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code NRA·June 29, 2022

OXFORD PKS CEMENTLESS TIBIA LEFT ALPHA POROUS/HA + EXTRACTOR SLOT LEFT MEDIAL SI

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code NRA·June 29, 2022

OXFORD PKS HIGH FLEX TWIN PEG CEMENTED FEMUR MEDIUM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code NRA·June 29, 2022

IMMULITE 2000

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CFP·January 23, 2012

IMMULITE 2000

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CFP·February 2, 2012

CORE IMPACTION DRILL

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·January 18, 2013

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIQ·December 13, 2010

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 14, 2014

IMMULITE 2000 INSULIN

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CFP·January 27, 2012

IMMULITE 2000 INSULIN

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CFP·February 1, 2012

Alcon Custom Pak

FDA Enforcement
Class II ·Ongoing·Alcon Research, LTD.·August 23, 2023