10 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ARROW ANATOMICAL SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450545102·
IMMUNOCARD STAT! E. COLI O157 PLUS
FDA 510(k)
FDA Class 1
·Microbiology
SMITH & NEPHEW SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
LINER AND SHELL WITH PLASTIC BARRIER 48 MM I.D. 60 MM O.D.
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·May 3, 2023
TRANSPAC IV MONITORING KIT W/SAFESET
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code DRS·March 11, 2016
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 6, 2013
LAMITRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 4, 2014
POLIGRIP
FDA Adverse Event
Other
·GLAXOSMITHKLINE·Product code KOL·April 15, 2011
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