77 results · 48ms · Sources: EU EUDAMED, US FDA

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MED LABS, INC.

FDA registration
MED LABS, INC.·3 products·🇺🇸 United States

EMS-1C

FDA UDI
Med Labs Inc·G395EMS1C1·Electronic Muscle Stimulator Interrupted DC

PA-1

FDA UDI
Med Labs Inc·G395PA11·Portable Alarm System communication . powered

EMS-2C

FDA UDI
Med Labs Inc·G395EMS2C1·Electronic Muscle Stimulator Interrupted DC and...

E-Z CALL

FDA UDI
Med Labs Inc·G395EZCALL1·Nurse Call Switch Communication System non-powered

MARQUETTE SOLAR 8000

FDA Adverse Event
Injury ·MARQUETTE MED. SYS.·Product code MHX·January 12, 1998

Medline Med-Checks BI Test packs with Instant Readout Integrator, SteriTec Product Code PL 200, Distributor Product Code MDS200500IR SteriTec Steam Biological Test Packs with Instant Readout Integrator Card: The Steam Biological Test Pack with Instant Readout Integrator is a steam sterilization monitor designed specifically for biological testing of pre-vacuum steam sterilizers operating at 132¿C (270¿F) for 3 minutes or longer. The Instant Readout Integrator Card gives the operator a prediction of the biological test outcome

FDA Enforcement
Class II ·Terminated·Steritec Products Mfc. Co., Inc.·August 7, 2013

BARD INTRA AORTIC BALLOON PUMP

FDA Adverse Event
Malfunction ·BARD·Product code DSP·March 7, 2003

SOFTHEAT

FDA Adverse Event
Other ·KAZ USA, INC.·Product code IRT·May 1, 2015

FORCE FX GENERATOR

FDA Adverse Event
VALLEYLAB, INC.·Product code GEI·May 10, 2000

ACCESS® 2 IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·March 8, 2011

INFUSOMAT

FDA Adverse Event
Injury ·B. BRAUN MELSUNGEN AG·Product code FRN·January 25, 2021

ACCESS 2 IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC·Product code MMI·December 12, 2008

AMBIT ELECTRONIC PAIN CONTROL PUMP

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code MEA·May 17, 2023

ACCESS® 2 IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code MMI·July 10, 2010

INAMED AESTHETICS BREAST IMPLANT

FDA Adverse Event
Injury ·INAMED/ ALLERGAN·Product code FTR·January 26, 2023

LEVEEN NEEDLE ELECTRODE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code GEI·July 17, 2007

THERMOCOOL SMART TOUCH SF BI-DIRECTIONAL NAVIGATION CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·May 26, 2021

THERMOCOOL SMART TOUCH SF BI-DIRECTIONAL NAVIGATION CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·May 26, 2021

DIALOG+® 

FDA Adverse Event
Injury ·B. BRAUN AVITUM, AG - MELSUNGEN·Product code KDI·September 14, 2017