28 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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INSTANT-VIEW MDMA (ECSTASY, XTC) URINE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Asst Vac Kit
FDA UDI
Engle Dental Systems, LLC·00850043433446·Central vacuum kit, fixed position
CarePoint Precision
FDA UDI
ALLISON MEDICAL, INC.·00786227225050·25G x 1" Poly Hub Needle
TIGER Spine System
FDA UDI
CORELINK LLC·M7256022501·5500 SERIES CONNECTOR - LEFT OFFSET - RETAININ...
TIGER Spine System
FDA UDI
CORELINK LLC·M72560225010·5500 SERIES CONNECTOR LEFT OFFSET RETAINING WAS...
36M - City of Gastonia - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588025018·36M - City of Gastonia - Metal
Lithotripsy Probe 1.9FR 250cm
FDA UDI
NORTHGATE TECHNOLOGIES INC.·00817183020059·1.9FR 250cm Lithotripsy Probe for use with Auto...
H.M.T. ACUPUNCTURE NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
V.A.C. INSTILLAMAT (VACUUM ASSISTED CLOSURE INSTILLAMAT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ONESTEP CPR AA
FDA Adverse Event
Malfunction
·BIO-DETEK INCORPORATED·Product code MKJ·December 1, 2025
OMNIPOD 5 AUTOMATED INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code QFG·June 13, 2024
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON INC·Product code OTN·March 27, 2013
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 14, 2014
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·February 15, 2011
FAST 1.1MM DRILLBIT MINIQUICK
FDA Adverse Event
Injury
·BIOMET TRAUMA·Product code HTW·June 1, 2017
PFC SIGMARP STB TB IN 3 10.0
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code NJL·December 29, 2021
PFC*SIGMA/RD/DOME PAT 3PEG,38
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 29, 2021
IMPELLA 5.5 WITH SMARTASSIST S2 SET, US
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code OZD·January 27, 2026
+3MM THICKNESS 40MM DIAMETER BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·August 22, 2023
M2A 38MM MOD HD +3MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 25, 2013