FDA.reportPublic FDA data

BioMonitor IV

Primary DI
04035479177850
Brand
BioMonitor IV
Company
BIOTRONIK SE & Co. KG
Model
471155
Catalog number
471155
Published
2023-05-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
MXDRecorder, Event, Implantable Cardiac, (With Arrhythmia Detection)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MXDRecorder, Event, Implantable Cardiac, (With Arrhythmia Detection)Cardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K230375000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K230375000BIOMONITOR IVBiotronik, Inc.2023-05-19MXD

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04035479177850PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04035479177850040354791778504035479177850

GMDN Terms#

Term, Definition table
TermDefinition
Implantable cardiac monitorA hermetically-sealed, electrically-powered device [an implantable cardiac monitor (ICM)] intended to be implanted to monitor, record, and store electrocardiographic signals to help diagnose and monitor cardiac arrhythmias and/or acute coronary syndrome (ACS) changes; it may have a vibratory alarm function and the data can be telemetrically transmitted to an external device for alarming the patient and/or remote data transmission. It is used for a patient who experiences unexplained cardiac-related symptoms and/or is at risk for cardiac arrhythmias and/or ACS events.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Temperature14 Degrees Fahrenheit113 Degrees Fahrenheit

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
315620229
Device count
1
Serial number
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04035479170295Tunneler L4578564578562026-05-28
04035479190538SW HMSC 3.664980924980922026-05-28
04035479182755Rivacor Sky DR-T4819824819822026-04-20
04035479182779Rivacor Sky VR-T DX4819834819832026-04-20
04035479182793Rivacor Sky VR-T4819844819842026-04-20
04035479182809Acticor Sky HF-T QP4819854819852026-04-20
04035479182816Acticor Sky HF-T4819864819862026-04-20
04035479182823Acticor Sky DR-T4819874819872026-04-20
04035479182830Acticor Sky VR-T DX4819884819882026-04-20
04035479182847Acticor Sky VR-T4819894819892026-04-20
04035479182854Rivacor Sky HF-T QP4819904819902026-04-20
04035479182861Rivacor Sky HF-T4819914819912026-04-20
04035479182984Rivacor Aura HF-T QP4820124820122026-04-20
04035479182991Rivacor Aura HF-T4820134820132026-04-20
04035479183004Rivacor Aura DR-T4820144820142026-04-20
04035479183011Rivacor Aura VR-T4820154820152026-04-20
04035479183028Rivacor Rise HF-T QP7820164820162026-04-20
04035479183035Rivacor Rise HF-T4820174820172026-04-20
04035479183042Rivacor Rise DR-T4820184820182026-04-20
04035479183059Rivacor Rise VR-T DX4820194820192026-04-20

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
05415067055095Assert-IQ™ST. JUDE MEDICAL, INC.MXD2026-01-05
05415067053275Merlin.net™ST. JUDE MEDICAL, INC.MXD2025-10-21
00802526618208myLUX™ Patient AppBOSTON SCIENTIFIC CORPORATIONMXD2025-04-11
00802526618215myLUX™ Patient AppBOSTON SCIENTIFIC CORPORATIONMXD2025-04-11
00802526625404LUX-Dx™BOSTON SCIENTIFIC CORPORATIONMXD2024-09-30
00763000754914CareLink SmartSync™ LINQ II™ Insertable Cardiac Monitor (ICM) ApplicationMEDTRONIC, INC.MXD2024-04-25
00763000891091CareLink SmartSync™ LINQ II™ Platform ApplicationMEDTRONIC, INC.MXD2024-04-25
00802526621017LUX-Dx™ Clinic Assistant Mobile DeviceBOSTON SCIENTIFIC CORPORATIONMXD2023-12-14
00763000613747LINQ II™MEDTRONIC, INC.MXD2023-11-19
00802526621000myLUX™ Mobile DeviceBOSTON SCIENTIFIC CORPORATIONMXD2023-09-08
00802526620706LUX-Dx II+™BOSTON SCIENTIFIC CORPORATIONMXD2023-08-31
00802526620713LUX-Dx II™BOSTON SCIENTIFIC CORPORATIONMXD2023-08-31
00802526621307myLUX™BOSTON SCIENTIFIC CORPORATIONMXD2023-08-31
00802526623103myLUX™ Patient AppBOSTON SCIENTIFIC CORPORATIONMXD2023-08-31
00802526623110myLUX™ Patient AppBOSTON SCIENTIFIC CORPORATIONMXD2023-08-31
00763000504519AccuRhythm™ AIMEDTRONIC, INC.MXD2021-12-31
00763000504526AccuRhythm™ AIMEDTRONIC, INC.MXD2021-12-31
00763000504533AccuRhythm™ AIMEDTRONIC, INC.MXD2021-12-31
00763000562625Reveal LINQ™MEDTRONIC, INC.MXD2021-09-04
00763000562632Reveal LINQ™MEDTRONIC, INC.MXD2021-09-04
00763000554002LINQ II™MEDTRONIC, INC.MXD2021-06-14
00763000060374LINQ II™MEDTRONIC, INC.MXD2020-07-18
00763000162191LINQ II™MEDTRONIC, INC.MXD2020-07-18
00802526607103LUX-Dx™ Insertable Cardiac MonitorBOSTON SCIENTIFIC CORPORATIONMXD2020-07-01
00802526607363myLUX™ Patient Kit with mobile deviceBOSTON SCIENTIFIC CORPORATIONMXD2020-07-01
00802526607370LUX-Dx™ Clinic Assistant Kit with mobile deviceBOSTON SCIENTIFIC CORPORATIONMXD2020-07-01
00802526607608myLUX™ patient appBOSTON SCIENTIFIC CORPORATIONMXD2020-07-01
00802526607615LUX-Dx™ Clinic Assistant appBOSTON SCIENTIFIC CORPORATIONMXD2020-07-01
00802526613838LATITUDE® ClarityBOSTON SCIENTIFIC CORPORATIONMXD2020-07-01
04035479169862BioMonitor IIImBIOTRONIK SE & Co. KGMXD2020-05-06