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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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Surgical Lights — 2 UDI-DI variants, MDR (SURGIRIS)

MD Atlas
SURGIRIS

Data from EUDAMED, last updated May 19, 2026

Surgical Lights

37015026000138

2 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: SURGIRIS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37015026000138
Device name: Surgical Lights
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: SURGIRIS
SRN: FR-MF-000004556
Country: France
Email: info@surgiris.com
Phone: +33 3 20 160793

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JNJTKYTG6TV2H3901956NCRQ

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

CEPURE-0103701502627210
CEPURE-02/J03701502627203