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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

LC 090M — Class I MDR by DASER S.r.l.

MD Atlas
DASER S.r.l.

EUDAMED last updated this device on Oct 23, 2025

LC 090M

805750267LC00355

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DASER S.r.l.
UDI-DI code: 08057502674859
Reference / catalog number: LC 090M

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View device family (Basic UDI)

Manufacturer information

Organization name: DASER S.r.l.
SRN: IT-MF-000030945
Manufacturer status: Active

Related devices

LC 093805750267LC00355On the market LC 093805750267LC00355On the market LC 095805750267LC00355On the market LC 097805750267LC00355On the market LCLK243074805750267LC00355On 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

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

CW011
Utilizzare sotto controllo medico
CW010
Utilizzare il dispositivo secondo le istruzioni (Modalità d'uso)

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08057502674859
Basic UDI-DI: 805750267LC00355
Reference / catalog number: LC 090M
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: 20
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

EMDN nomenclature code(s)

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

V0804PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures)

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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