11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDLINE SURGICAL GOWNS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Heater for Coupling Gel
FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904090085·
MEDIPORT 2000 MOBILE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FLOSTAR NEEDLELESS CONNECTOR, MODEL FS3000
FDA 510(k)
FDA Class 2
·General Hospital
S-ROM*HEAD FEMORAL COCR 32+6
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 19, 2024
SYNFRAME HALF RING
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code LXH·June 8, 2015
IBP ELB INT. ULNA LRG RGT LNG STM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·June 24, 2016
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·April 9, 2013
RESTORE PRIME ADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 28, 2011
FINELINE II
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code DTB·May 8, 2008
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