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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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CONSULTATION UNIT ONE-I — 2 UDI-DI variants, MDR (NIDEK SA)

MD Atlas
NIDEK SA

Data from EUDAMED, last updated May 19, 2026

CONSULTATION UNIT ONE-I

37008623UCO007BT

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: NIDEK SA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37008623UCO007BT
Device name: CONSULTATION UNIT ONE-I
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: NIDEK SA
SRN: FR-MF-000000493
Country: France
Email: site@nidek.fr
Phone: +33 1 49 80 97 97

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JC0JPQ2WH7E4Q10VFG81VBRW

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

ONE-I Plateau à élévation motorisée03700862300047
ONE-I Plateau hauteur fixe03700862300016