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Organization name
UDI-DI code
Reference / catalog number

ANGELO 200 XL ABRICOT — Class I MDR by VILGO

MD Atlas
VILGO

EUDAMED last updated this device on Mar 31, 2026

ANGELO 200 XL ABRICOT

361580ANGELO200XLVK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VILGO
UDI-DI code: 03615800045457
Reference / catalog number: 1060044S11

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Manufacturer information

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

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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: ANGELO 200 XL ABRICOT
UDI-DI code: 03615800045457
Basic UDI-DI: 361580ANGELO200XLVK
Reference / catalog number: 1060044S11
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: DEAMBULATEUR REF ANGELO 200 XL ABRICOT - ACIER EPOXY ABRICOT 2012 RENFORCE 2 ROUES PLIANT AVEC SIEGE TAILLE XL
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y120606WHEELED WALKER

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

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.