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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

M5000IMB — Class I MDR by Service Med Srl

MD Atlas
Service Med Srl

EUDAMED last updated this device on Apr 13, 2026

M5000IMB

805572850MASSMIJU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Service Med Srl
UDI-DI code: 08055728500181
Reference / catalog number: M5000IMB

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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

Certificates

Certificate health across this manufacturer's portfolio.

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

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: 08055728500181
Basic UDI-DI: 805572850MASSMIJU
Reference / catalog number: M5000IMB
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: LENGHT 200 CM, WIDTH 120 CM, H 18 CM

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.

V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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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