10,000 results · 69ms · Sources: EU EUDAMED, 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