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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

ET0012 — Class I MDR by Praesidia S.r.l.

MD Atlas
Praesidia S.r.l.

EUDAMED last updated this device on May 22, 2026

ET0012

803367578ECOTHERM87

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Praesidia S.r.l.
UDI-DI code: 08033675780382
Reference / catalog number: ET0012

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View device family (Basic UDI)

Manufacturer information

Organization name: Praesidia S.r.l.
SRN: IT-MF-000010975
Manufacturer status: Active

Related devices

ET0014803367578ECOTHERM87On the market ET0018803367578ECOTHERM87On the market ET0115803367578ECOTHERM87On the market ET0011803367578ECOTHERM87On the market ETSF001803367578ETSECUREFOAMRJOn the market

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

3 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
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 26, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08033675780382
Basic UDI-DI: 803367578ECOTHERM87
Reference / catalog number: ET0012
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: 80
Additional product description: —
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)08033675780382

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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.

T020103SURGICAL THERMAL DRAPES

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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