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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 AFFINITY — 2 UDI-DI variants, MDR (NIDEK SA)

MD Atlas
NIDEK SA

Data from EUDAMED, last updated May 19, 2026

Consultation Unit AFFINITY

37008623UCO005BP

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: 37008623UCO005BP
Device name: Consultation Unit AFFINITY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 29, 2021

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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Export results

Applied filters

basicUdiUlid01FR3GB8V51NAGV411T4TQYHD6

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

Unité de consultation AFFINITY03700862300160
Unité de consultation AFFINITY RT03700862300177