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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

Mars - Mercurius — Class IIa MDD by Rossiello Angelo

MD Atlas
Rossiello Angelo

EUDAMED last updated this device on Oct 27, 2022

Mars - Mercurius

B-EliosLampN7

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Rossiello Angelo
UDI-DI code: D-EliosLampN7
Reference / catalog number: Mars - Mercurius

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View device family (Basic UDI)

Manufacturer information

Organization name: Rossiello Angelo
SRN: IT-MF-000028481
Manufacturer status: Inactive

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	Apr 23, 2021	May 26, 2024

Device identification

Trade name: not provided
UDI-DI code: D-EliosLampN7
Basic UDI-DI: B-EliosLampN7
Reference / catalog number: Mars - Mercurius
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC 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: 15 MU10
43 MU10
44 MU10
4.5 MU29

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-EliosLampN7

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

Z120614INFRARED ULTRAVIOLET RAY LAMPS

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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Related devices

This device is not currently linked to any other device.

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.