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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

LIFTY PROMEFA - GRIS 7001/7031 -… — Class I MDR by VILGO

MD Atlas
VILGO

EUDAMED last updated this device on Apr 1, 2026

LIFTY PROMEFA - GRIS 7001/7031 - SANS SANGLE

361580LIFTYB7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VILGO
UDI-DI code: 03615800049165
Reference / catalog number: 5010077S03

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Manufacturer information

Organization name: VILGO
SRN: FR-MF-000009712
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: LIFTY PROMEFA - GRIS 7001/7031 - SANS SANGLE
UDI-DI code: 03615800049165
Basic UDI-DI: 361580LIFTYB7
Reference / catalog number: 5010077S03
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: LEVE PERSONNE ELECTRIQUE REF LIFTY PROMEFA - CHASSIS ACIER EPOXY BICOLORE GRIS 7001-7031 / FLEAU 4 POINTS PROMEFA / SANS SANGLE
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0805030102ELECTRIC MOBILE LIFTS

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

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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.