15 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISCOVERY MR750 3.0T ,DISCOVERY MR450 1.5T, DISCOVERY MR750 3.0T,OPTIMA MR450W 1.5T
FDA 510(k)
FDA Class 2
·Radiology
CRONO F
FDA 510(k)
FDA Class 2
·General Hospital
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
FDA 510(k)
FDA Class 1
·General Hospital
SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
FDA Adverse Event
Injury
·SYNTHES USA·Product code MQP·November 10, 2017
SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
FDA Adverse Event
Injury
·SYNTHES USA·Product code MQP·November 10, 2017
IMP,TSV,4.1MM,DUAL SEL,HA
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·February 5, 2024
S-ROM*STM STD,30 NK,16X11X150
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 3, 2013
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SAO PAULO·Product code KDI·June 28, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 3, 2008
IMPL TAPERED SCR-V SBM 3.7MM 3.5MM 10MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·February 5, 2024
UNIVERSA LOOP NEPHROSTOMY PERCUTANEOUS DRAINAGE CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KOB·May 2, 2018
UNKNOWN_SPINE_PRODUCT
FDA Adverse Event
Injury
·Product code HSB·June 21, 2021
UNKNOWN_SPINE_PRODUCT
FDA Adverse Event
Injury
·STRYKER SPINE-US·Product code MQP·June 21, 2021
UNKNOWN_SPINE_PRODUCT
FDA Adverse Event
Injury
·STRYKER SPINE-US·Product code KWP·June 21, 2021
Shaver Handpiece Sterilization Tray. Model number 272-700-000. For sterilization of Stryker Endoscopy arthroscopic shaver.
FDA Enforcement
Class II
·Terminated·Stryker Endoscopy·July 2, 2014