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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Umana T1 Heart Monitor — 1 UDI-DI variant, MDD

MD Atlas
Umana Medical Technologies Ltd

Data from EUDAMED, last updated May 31, 2026

Umana T1 Heart Monitor

B-05350627999979

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Umana Medical Technologies Ltd

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: 423-00-02-DM
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ITALCERT SRL (0426)
Validity: Jan 30, 2024

Identity & classification

Basic UDI-DI: B-05350627999979
Device name: Umana T1 Heart Monitor
Device model: UMT-T102
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Feb 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: Umana Medical Technologies Ltd
SRN: MT-MF-000018092
Country: Malta
Email: info@umanamedical.com
Phone: +356 2763 9710

Variants by status

UDI-DI variants

1 UDI-DI variant

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Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Umana T1 Heart Monitor05350627999979