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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

549 BIS VERT — Class I MDR by VILGO

MD Atlas
VILGO

EUDAMED last updated this device on Mar 10, 2026

549 BIS VERT

361580549PH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VILGO
UDI-DI code: 03615800012206
Reference / catalog number: 1040006S7

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Manufacturer information

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

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2 - 80 cm3615802YFOn the market 2 - 87,5cm3615802YFOn the market 2 - 95cm3615802YFOn the market 3 - 80 cm3615803YHOn the market 3 - 87,5cm3615803YHOn 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 France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: 549 BIS VERT
UDI-DI code: 03615800012206
Basic UDI-DI: 361580549PH
Reference / catalog number: 1040006S7
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: TRIPODE REF 549 BIS VERT - ACIER EPOXY VERT 6026 POIGNEE COL DE CYGNE
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y120315TRIPODS

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

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Expiration date
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