Unified Care+

Primary DI
00850044118939
Brand
Unified Care+
Company
iHealth Labs Inc.
Model
1.5
Device description
This is stand alone software intended for use in the home and clinical settings as an aid for users and their healthcare professionals to view test results which are measured by iHealth devices to better manage user's health and get feedback from their professional care team. It can also connect to medical devices and/or non-medical devices and get data from devices during measurement or from the data stored in memory of the device for enhanced data managements. Data can be transmitted, displayed, and stored in the App.
Published
2026-05-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true

Product Codes#

Code, Name table
CodeName
MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)Cardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K243146000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K243146000iCare APPIhealth Labs, Inc.2025-02-03MWI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850044118939PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850044118939008500441189398500441189390850044118939

GMDN Terms#

Term, Definition table
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.

Regulatory Flags#

DUNS number
054953337
Device count
1

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850044118045iHealthICO-30002022-09-30
00850044118236iHealthBG5SKIT2024-05-28
00850044118243iHealthBG5SKIT2024-05-27
00856362005043iHealthPT32020-07-31
00856362005159iHealthBG5SKIT2025-12-19
00850044118083iHealthPT32023-08-14
00850044118007iHealthKD-7232022-09-29
00850044118205iHealthEGS-20032023-08-24
00850044118250iHealthEGS-20032023-08-30
00850044118267iHealthEGS-20032023-08-30
00850044118694iHealthPT2L2025-12-19
00850044118700iHealthPT9L2025-12-19
00850044118724iHealthPT9L2025-12-19
00850044118823iHealthKD-5811BT2026-04-15
00850044118830iHealthKD-5811BT2026-04-15
00850044118960iHealthBP-300CL2025-12-10
00850078377081iHealthKN-550BT2025-12-19
00855111003279iHealthPO32023-08-14
00855111003958iHealthBP3L2022-09-30
00856362005005iHealthKN-550BT2022-10-01

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Primary DI, Brand, Company table
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00850086928022SENSINEL™ CARDIOPULMONARY MANAGEMENT (CPM) SYSTEM)Analog Devices, Inc.MWI2026-06-03
00850086928039SENSINEL™ CARDIOPULMONARY MANAGEMENT (CPM) SYSTEM)Analog Devices, Inc.MWI2026-06-03
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