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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

4911007100 — Class IIb MDR by Meditalia Industriale Srl

MD Atlas
Meditalia Industriale Srl

EUDAMED last updated this device on May 28, 2026

4911007100

805848056Transfer49

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Meditalia Industriale Srl
UDI-DI code: 08058480560295
Reference / catalog number: 4911007100

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View device family (Basic UDI)

Manufacturer information

Organization name: Meditalia Industriale Srl
SRN: IT-MF-000032344
Manufacturer status: Active

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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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	May 31, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08058480560295
Basic UDI-DI: 805848056Transfer49
Reference / catalog number: 4911007100
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: I dispositivi medici Solutran®hemo sistemi accessori , appartengono alla linea di dispositivi medici denominata “Sistemi Accessori” del Fabbricante Meditalia Industriale S.r.l. Sono dispositivi medici costituiti da sistemi di sacche in PVC di diversi volumi, completi di tubi e raccordi, ognuno destinato ad una specifica attività relativa ad emocomponenti, come ad esempio: stoccaggio, trasferimento, conservazione e preparazione di emocomponenti. Nello specifico comprendono: 1. Sistema di sacche per trasferimento e stoccaggio di aliquote di: A. Piastrine B. Plasma C. Globuli rossi 2. Sacche singole per trasferimento e stoccaggio di: A. Piastrine B. Emocomponenti (Blood Components) C. Globuli rossi 3. Sistema per la preparazione di pool. A. Per crioprecipitato
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

EMDN nomenclature code(s)

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

B010201WHOLE BLOOD, RED BLOOD CELLS OR PLASMA TRANSFER BAGS AND KITS

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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