14 results · 35ms · Sources: EU EUDAMED, US FDA

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CDC ANAEROBE BLOOD AGAR

FDA 510(k)
FDA Class 1 ·Microbiology

PLATE CDC ANAEROBE 5% SB 100 EA JP

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·September 9, 2021

PLATE CDC ANAEROBE 5% SB 20 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSG·June 28, 2021

PLATE CDC ANAEROBE AGAR 5% SB 90MM 20

FDA Adverse Event
Malfunction ·BECTON DICKINSON GMBH·Product code JSG·February 17, 2022

Leica Biosystems

FDA UDI
Leica Biosystems Richmond, Inc.·10849832024276·CLEAR BASE MOLDS 15 x 15, 400 Count

Signature III

FDA UDI
Rmo, Inc.·00885797101655·SIG III ROTH .018 5-5 HK CUS

MetaSystems Probes

FDA UDI
MetaSystems Probes GmbH·04251315808331·XCE 3 orange, 4x conc., Centromere-Specific Probe

MetaSystems Probes

FDA UDI
MetaSystems Probes GmbH·04251315808232·XCE 3 red, 4x conc., Centromere-Specific Probe

GIVEN PILLCAM PLATFORM WITH RAPID 6.5 / GIVEN PILLCAM PLATFORM WITH PILLCAM ESO 3 CAPSULES

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

SYNTHES 4.5 MM VA-LCP CURVED CONDYLAR SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ECHELON LINEAR CUTTER RELOAD

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 9, 2014

ALARIS PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Injury ·CAREFUSION CORP·Product code FPA·October 17, 2012

ELECSYS 2010 RACK

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS CORPORATION·Product code MMI·August 17, 2010

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012