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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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C15 BIS — 11 UDI-DI variants, MDR (VILGO)

MD Atlas
VILGO

Data from EUDAMED, last updated May 19, 2026

C15 BIS

361580C15BISLN

11 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: 361580C15BISLN
Device name: C15 BIS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 28, 2026

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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KG2SNF7F7SPZAYXF40QJDCFZ

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

C15 BIS BLEU03615800011513
C15 BIS BLEU PASTEL03615800011377
C15 BIS BLEU VERT03615800041459
C15 BIS GRIS PASTEL03615800011384
C15 BIS LAGON03615800041442
C15 BIS LILAS03615800011407
C15 BIS NOIR03615800000845
C15 BIS NOIR DECOR03615800011421
C15 BIS ROSE03615800011414
C15 BIS ROUGE03615800011438
C15 BIS VERT PASTEL03615800011391