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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

L10G — Class I MDR by DF MEDICA Oone srl

MD Atlas
DF MEDICA Oone srl

EUDAMED last updated this device on Apr 3, 2026

L10G

805699498Z120606KA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DF MEDICA Oone srl
UDI-DI code: 08056994983586
Reference / catalog number: L10G

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View device family (Basic UDI)

Manufacturer information

Organization name: DF MEDICA Oone srl
SRN: IT-MF-000028375
Manufacturer status: Active

Related devices

BG04HP805699498FT002DOQFOn the market BU02HP805699498FT002DOQFOn the market BG16HP805699498FT002DOQFOn the market BS07805699498FT003DOQLOn the market L03SG805699498Z120606KAOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08056994983586
Basic UDI-DI: 805699498Z120606KA
Reference / catalog number: L10G
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)08056994983586

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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.

Z120606MAGNETOTHERAPY EQUIPMENT

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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