Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

549 BIS ABRICOT — Class I MDR by VILGO

MD Atlas
VILGO

EUDAMED last updated this device on Mar 10, 2026

549 BIS ABRICOT

361580549PH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VILGO
UDI-DI code: 03615800012268
Reference / catalog number: 1040006S13

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

2 - 80 cm3615802YFOn the market 2 - 87,5cm3615802YFOn the market 2 - 95cm3615802YFOn the market 3 - 80 cm3615803YHOn the market 3 - 87,5cm3615803YHOn the market

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 ABRICOT
UDI-DI code: 03615800012268
Basic UDI-DI: 361580549PH
Reference / catalog number: 1040006S13
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 ABRICOT - ACIER EPOXY ABRICOT 2012 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

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.