FDA.report

myoncare

Primary DI
04260658860234
Brand
myoncare
Company
ONCARE GmbH
Model
1.13
Published
2025-11-26
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Product Codes

CodeName
OUGMedical Device Data System

Product Code Classifications

CodeDeviceSpecialtyClass
OUGMedical Device Data SystemGeneral Hospital1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
04260658860234PrimaryGS10

GMDN Terms

TermDefinition
Self-care monitoring/reporting softwareAn application software program designed for the continual collection and aggregation of a patient's self-care data to promote communication between patient and healthcare provider, to facilitate a patient's self-care by using rules defined during use of the application, and/or to facilitate population monitoring. It is typically used to capture clinical (e.g., blood pressure, weight, and blood glucose), nutritional, and/or exercise information in the home, which may include medication administration information captured from enabled injection devices and data from wearable devices, providing care plan, journal, medication advice, and/or messaging functionalities.

Sterilization Methods

Method

Regulatory Flags

DUNS number
313530563
Device count
1
DM exempt
true
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company

Primary DIBrandModelCatalogPublished
04260658860203myoncare1.122025-06-30
04260658860173myoncare1.112024-12-17
04260658860142myoncare1.102024-07-29
04260658860111myoncare1.92023-12-18
04260658860081myoncare1.82023-06-16
04260658860067myoncare1.72023-02-16
04260658860043myoncare1.6.22022-11-04

Other Devices Sharing Product Codes

Primary DIBrandCompanyProduct codePublished
05404028001158Mimics FlowMaterialise NVOUG2026-03-23
05404028001172SurgiCase OnlineMaterialise NVOUG2026-03-23
05404028001189ProPlan CMF Materialise NVOUG2026-03-23
00763000994914NAMEDTRONIC, INC.OUG2026-03-22
00382904450106BD Veritor™ InfoWiFi ModuleBECTON, DICKINSON AND COMPANYOUG2026-03-13
04035479189211PatientApp 2.9BIOTRONIK SE & Co. KGOUG2026-03-04
07350149360033PD Care SystemPainDrainer ABOUG2026-03-04
00860015454706RocotoRocoto Inc.OUG2026-02-26
00860015454713RocotoRocoto Inc.OUG2026-02-26
00860015454720RocotoRocoto Inc.OUG2026-02-26
00860015454737RocotoRocoto Inc.OUG2026-02-26
00860015454768RocotoRocoto Inc.OUG2026-02-26
00860015454775RocotoRocoto Inc.OUG2026-02-26
00840241600412Kestra Provided Device Patient ApplicationKestra Medical Technologies, Inc.OUG2026-02-04
00199150002184NAMEDTRONIC, INC.OUG2026-02-01
03770034761006LIMSTARHOPI MEDICALOUG2026-01-28
03770034761013MINILIMHOPI MEDICALOUG2026-01-28
03770034761020FMCHOPI MEDICALOUG2026-01-28
03770034761037HOPACKHOPI MEDICALOUG2026-01-28
03770034761044SATCHELHOPI MEDICALOUG2026-01-28
05056190500658SafeIDVISION RT LIMITEDOUG2025-12-23
00850064210286ANNE Link MobileSibel Health Inc.OUG2025-12-11
15099590799243MicroScanBeckman Coulter, Inc.OUG2025-12-08
15099590799250MicroScanBeckman Coulter, Inc.OUG2025-12-08
15099590807146MicroScanBeckman Coulter, Inc.OUG2025-12-08
00199284197749ActuviActuvi LLCOUG2025-12-02
07350149360026PD Care SystemPainDrainer ABOUG2025-11-13
04961333255696Digital Capture v3.7.0PENTAX OF AMERICA, INC.OUG2025-09-12
00763000274559N/AMEDTRONIC, INC.OUG2025-09-05
04260657690726MLC-SADLINK Technology GmbHOUG2025-08-31