33 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Needleless Connector
FDA 510(k)
FDA Class 2
·General Hospital
VERSALOOP™ XL Straight Guide for 1.5mm Anchor XL, Sawtooth
FDA UDI
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10818674025062·
10PW - Penn Power & Light
FDA UDI
Certified Safety Manufacturing, Inc.·00766588012179·10PW - Penn Power & Light
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319721872·Cinelli Osteotome 6-1/2" (16.3cm), 14mm cut, do...
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345024007·PADDLE SPREADER, 17MM
VIDAS D-DIMER EXCLUSION II 60T
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code DAP·June 19, 2020
4 PORT, 4 WAY STOPCOCK
FDA 510(k)
FDA Class 2
·General Hospital
SONICSTIMU COMBO THERAPEUTIC DEVICE
FDA 510(k)
FDA Class 2
·Physical Medicine
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·March 8, 2023
T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·January 16, 2025
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 5, 2025
LM
FDA Adverse Event
Malfunction
·YANGZHOU MEDLINE INDUSTRY CO, LTD.·Product code MEG·March 25, 2021
PUMP MMT-712LNAL PRDGM INS CL EN US LN
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·October 22, 2008
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 27, 2013
IN TOUCH ZU
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·July 11, 2011
NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·September 28, 2022
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·December 27, 2024
UNK - IMPLANTS
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·October 28, 2019
UNK - IMPLANTS
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·October 28, 2019
Surpria 64: Software Version V3.11, V3.22
FDA Enforcement
Class II
·Ongoing·FUJIFILM Healthcare Americas Corporation·September 21, 2022