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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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LISA - Trial Spacer — 4 UDI-DI variants, MDR (BACKBONE)

MD Atlas
BACKBONE

Data from EUDAMED, last updated May 19, 2026

LISA - Trial Spacer

376024863LISA204G6

4 UDI-DI variants

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

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

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Device characteristics

Reusable

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 376024863LISA204G6
Device name: LISA - Trial Spacer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: BACKBONE
SRN: FR-MF-000001874
Country: France
Email: quality.regulatory@backbone.pro

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GSTDZ305Y6MJQZEJECKV6QVW

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

LISA - Trial Spacer (Size 6)03760248630069
LISA - Trial Spacer Size 1003760248630083
LISA - Trial Spacer Size 1203760248630090
LISA - Trial Spacer Size 803760248630076