10,000 results
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69ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DiamondTemp™ EGM cable
FDA UDI
MEDTRONIC NAVIGATION, INC.·00763000455699·EGM CABLE CEDTEGM100 DIAMONDTEMP US
Recording System EGM Cable
FDA UDI
BOSTON SCIENTIFIC CORPORATION·08714729270010·Non-Sterile Cable
ENDOTHELIAL GROWTH MEDIUM (EGM)
FDA 510(k)
FDA Class 1
·Hematology
ENDO TOOL GLUCOSE MANAGEMENT SYSTEM (EGMS)
FDA 510(k)
FDA Class 2
·Anesthesiology
Edema Guard Monitor (EGM) CardioSet-001
FDA 510(k)
FDA Class 2
·Cardiovascular
EGM
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code NVY·August 12, 2023
EGM CABLE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC, EP TECHNOLOGIES·Product code DSA·July 2, 2008
EGM CABLE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC, EP TECHNOLOGIES·Product code DSA·July 2, 2008
EGM-2 Singlequots w/o GA and Serum
FDA UDI
Lonza Walkersville, Inc.·00840075401827·
MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER; CARDIAC PATHWAYS EGM ADAPTER CABLES
FDA 510(k)
FDA Class 2
·Cardiovascular
AMPERE GENERATOR EGM 4 LEAD CABLE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code OAD·August 20, 2020
FARASTAR RECORDING SYSTEM MODULE EGM INPUT MODULE
FDA Adverse Event
Malfunction
·FARAPULSE, INC.·Product code QZI·August 22, 2024
MEDI-JECT
FDA Adverse Event
Other
·MEDI-JECT CORPORATION·Product code EGM·August 29, 1997
LIGEJECT
FDA Adverse Event
Other
·MILTEX INSTRUMENT CO.·Product code EGM·October 25, 1995
MADAJET XL
FDA Adverse Event
Injury
·MADA MEDICAL PRODUCTS, INC.·Product code EGM·September 18, 2017
MADAJET XL
FDA Adverse Event
Injury
·MADA MEDICAL PRODUCTS, INC.·Product code EGM·August 7, 2001
Model 3300 LATITUDE Programming System with installed Model 3892 ALTRUA, INSIGNIA I, NEXUS I Software Support Application
FDA Enforcement
Class II
·Terminated·Boston Scientific Corporation·November 11, 2020
ORCHESTRA
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code DXY·March 20, 2017
PARADYM
FDA Adverse Event
Injury
·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code NIK·July 24, 2015
ASSERT-IQ¿ ICM
FDA Adverse Event
Malfunction
·ABBOTT·Product code MXC·August 18, 2025