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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 111 — Class I MDR by DASER S.r.l.

MD Atlas
DASER S.r.l.

EUDAMED last updated this device on Oct 23, 2025

LC 111

805750267LC00355

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DASER S.r.l.
UDI-DI code: 08057502672824
Reference / catalog number: LC 111

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View device family (Basic UDI)

Manufacturer information

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

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

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: 08057502672824
Basic UDI-DI: 805750267LC00355
Reference / catalog number: LC 111
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: 10
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)08057502672824

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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.

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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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.