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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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Organization name
UDI-DI code
Reference / catalog number

01/03/2024 — Class I MDR by Telemedware srl

MD Atlas
Telemedware srl

EUDAMED last updated this device on Apr 7, 2026

01/03/2024

8058301590005ZG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Telemedware srl
UDI-DI code: 80583015900054
Reference / catalog number: 01/03/2024

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View device family (Basic UDI)

Manufacturer information

Organization name: Telemedware srl
SRN: IT-MF-000040590
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 80583015900054
Basic UDI-DI: 8058301590005ZG
Reference / catalog number: 01/03/2024
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Descrizione generale del dispositivo Il dispositivo oggetto della presente Documentazione Tecnica è un modulo software denominato “Gestione Terapia Medica”, parte della piattaforma TMED. Il modulo è progettato per supportare il personale sanitario nella gestione della terapia farmacologica, mediante funzionalità software dedicate al supporto della prescrizione, alla gestione della pianificazione delle somministrazioni e alla tracciabilità della terapia. Il presente STED si applica esclusivamente al modulo “Gestione Terapia Medica”. Le altre funzionalità della piattaforma TMED non rientrano nell’ambito della presente documentazione tecnica. Destinazione d’uso e utilizzatori previsti Il modulo “Gestione Terapia Medica” è destinato all’uso da parte di personale sanitario qualificato, quali medici e operatori sanitari autorizzati, in contesti clinici e assistenziali.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)80583015900054

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12040292GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.