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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

AD00013T — Class I MDR by Service Med Srl

MD Atlas
Service Med Srl

EUDAMED last updated this device on Apr 15, 2026

AD00013T

805572850AUSSMILU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Service Med Srl
UDI-DI code: 08055728500259
Reference / catalog number: AD00013T

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View device family (Basic UDI)

Manufacturer information

Organization name: Service Med Srl
SRN: IT-MF-000021629
Manufacturer status: Active

Related devices

RD300142805572850CUSSMIMNOn the market SG300141805572850CUSSMIMNOn the market SG300143805572850CUSSMIMNOn the market TCAREB44805572850CUSSMIMNOn the market TCARE044805572850CUSSMIMNOn the market

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	Jan 1, 2026	Dec 31, 2039

Device identification

Trade name: not provided
UDI-DI code: 08055728500259
Basic UDI-DI: 805572850AUSSMILU
Reference / catalog number: AD00013T
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: —
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)08055728500259

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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.

Y122406BELTS, SEATS AND ARMRESTS FOR WHEELCHAIRS

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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Certificates

Certificate health across this manufacturer's portfolio.

ITD 1450757 1Supplemented
Quality assuranceNotified body: 1936Expiry: Jan 26, 2028