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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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GR 171 — 34 UDI-DI variants, MDR (VILGO)

MD Atlas
VILGO

Data from EUDAMED, last updated May 19, 2026

GR 171

361580GR17139

34 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: 361580GR17139
Device name: GR 171
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 31, 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

34 UDI-DI variants

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Applied filters

basicUdiUlid01KN27285TEJX5WA7ST3QVNARH

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

GR 171 (NOIR/BORDEAUX)03615800022151
GR 171 (NOIR/NOIR)03615800022083
GR 171 (ROUGE/BLEU)03615800022274
GR 171 (ROUGE/NOIR)03615800022304
GR 171 (TURQUOISE/NOIR)03615800046126
GR 171 (VERT/BLEU)03615800022199
GR 171 (VERT/BORDEAUX)03615800022250
GR 171 (VERT/NOIR)03615800022168
GR 171 (VIOLET POURPRE/NOIR)03615800022328

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