16 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TORSO ARRAY COIL, MODEL 558GE-64
FDA 510(k)
FDA Class 2
·Radiology
SPROTTE® Sono
FDA UDI
Pajunk GmbH Medizintechnologie·14048223029470·SPROTTE® Sono
25G x ...
BQ+
FDA UDI
BQ PLUS MEDICAL CO., LTD.·16972620111187·
BQ+
FDA UDI
BQ PLUS MEDICAL CO., LTD.·06972620111173·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867427150·Dilator, 4.1 x 185mm
PSYCHEMEDICS RIA METHAMPHETAMINE AND MDMA ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
POLYPROPYLENE, NONABSORBABLE SURGICAL SUTURES USP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·February 15, 2019
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·February 15, 2019
TIBIAL PLATE FB SZ 1 LT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code HSN·January 31, 2024
SWEET PICOTIP
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·April 8, 2013
TAPERED DRILL
FDA Adverse Event
Injury
·STRYKER INSTRUMENTS CORK·Product code DZJ·March 29, 2011
PROGRAMMING WAND
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·May 9, 2008
M-LNCS Y-I
FDA Adverse Event
Malfunction
·MASIMO - 40 PARKER·Product code DQA·August 12, 2017
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
The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018