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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

SF2254DROSSA — Class IIa MDR by Dispotech srl

MD Atlas
Dispotech srl

EUDAMED last updated this device on May 18, 2026

SF2254DROSSA

++G066SFDIS6Z

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dispotech srl
UDI-DI code: G066SF2254DROSSA0
Reference / catalog number: SF2254DROSSA

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View device family (Basic UDI)

Manufacturer information

Organization name: Dispotech srl
SRN: IT-MF-000010735
Manufacturer status: Active

Certificates

Certificate health across this manufacturer's portfolio.

ITD 1344523 1Supplemented
Quality assuranceNotified body: 1936Expiry: Jul 29, 2029

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 3 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Germany		Still on market
France		Still on market

Device identification

Trade name: not provided
UDI-DI code: G066SF2254DROSSA0
Basic UDI-DI: ++G066SFDIS6Z
Reference / catalog number: SF2254DROSSA
Issuing entity: HIBCC

Classification

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

Device details

Quantity: 1
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

G066SF2254DROSSA0

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

M9001CRYOTHERAPY AND THERMOTHERAPY DEVICES

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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