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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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Lit parc — 17 UDI-DI variants, MDR (VILLARD)

MD Atlas
VILLARD

Data from EUDAMED, last updated May 19, 2026

Lit parc

37014191906LP

17 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: VILLARD

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37014191906LP
Device name: —
Device model: Lit parc
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: VILLARD
SRN: FR-MF-000002454
Country: France
Email: direction@villard-medical.com
Phone: +33 285290500

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01K9YXVZXNE1CYXYZYYFYV3SKF

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

505.5703701419100547
505.6103701419100585
505.6003701419100578
505.6203701419100592
505.6703701419100646
505.5403701419100523
505.5903701419100561
505.59SP203701419120200
505.6303701419100608
505.6403701419100615
505.6803701419100653
505.6903701419100660
505.5203701419100516
505.5603701419100530
505.6503701419100622
505.6603701419100639
505.5803701419100554