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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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571 — 19 UDI-DI variants, MDR (VILGO)

MD Atlas
VILGO

Data from EUDAMED, last updated May 19, 2026

571

361580571PA

19 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: VILGO

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 361580571PA
Device name: 571
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: VILGO
SRN: FR-MF-000009712
Country: France
Email: vilgo@hms-vilgo.com
Phone: +33 553744550

Variants by status

UDI-DI variants

19 UDI-DI variants

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Applied filters

basicUdiUlid01KBHRMZ6CVY7CR6GBNYKYQNZV

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

571 ABRICOT03615800008568
571 AMANDE03615800008537
571 BLANC03615800008636
571 BLEU03615800000203
571 BLEU PASTEL03615800008520
571 BLEU VERT03615800051861
571 BORDEAUX03615800046089
571 BRONZE03615800008650
571 GRIS PASTEL03615800008629
571 JAUNE03615800008544
571 LAGON03615800008575
571 LILAS03615800008599
571 NOIR03615800008612
571 NOIR DECOR03615800008643
571 ROSE03615800008551
571 ROUGE03615800006847
571 TURQUOISE03615800046331
571 VERT03615800008582
571 VERT PASTEL03615800008605