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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

LFZ00478 — Class IIb MDD by LIFEAZ SAS

MD Atlas
LIFEAZ SAS

EUDAMED last updated this device on Feb 4, 2025

LFZ00478

B-03770022399259

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: LIFEAZ SAS
UDI-DI code: 03770022399259
Reference / catalog number: LFZ00478

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Manufacturer information

Organization name: LIFEAZ SAS
SRN: FR-MF-000009348
Manufacturer status: Active

Related devices

LFZ00477B-03770022399235On the market LFZ00531B-03770022399440On the market LFZ00494B-03770022399037On the market LFZ00499B-03770022399310On the market LFZ00474B-03770022399150On 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.

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: 03770022399259
Basic UDI-DI: B-03770022399259
Reference / catalog number: LFZ00478
Issuing entity: GS1

Classification

Risk category: Class IIb
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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12030503AUTOMATIC DEFIBRILLATORS

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification