15 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CDC ANAEROBE BLD AGAR W/KANAMYCIN ETC.
FDA 510(k)
FDA Class 1
·Microbiology
Signature III
FDA UDI
Rmo, Inc.·00885797101631·SIG III ROTH .018, 12 BRKT KIT
KIM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AERONEB PORTABLE NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
NA
FDA UDI
Zimmer, Inc.·00889024132900·
NA
FDA UDI
Zimmer, Inc.·00889024132894·
NA
FDA UDI
Zimmer, Inc.·00889024132917·
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
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·May 9, 2014
STIMULATOR, BONE GROWTH, NON-INVASIVE
FDA Adverse Event
Injury
·ORTHOFIX INC.·Product code LOF·October 17, 2012
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·August 17, 2010
PLATE CDC ANAEROBE AGAR 5% SB 90MM 20
FDA Adverse Event
Malfunction
·BECTON DICKINSON GMBH·Product code JSG·February 17, 2022
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
Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018