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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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Néa Duo — 2 UDI-DI variants, MDR (SEFAM)

MD Atlas
SEFAM

Data from EUDAMED, last updated May 19, 2026

Néa Duo

3700659417029A

2 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: SEFAM

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3700659417029A
Device name: Néa Duo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: SEFAM
SRN: FR-MF-000009061
Country: France
Email: regulatoryaffairs@sefam-medical.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KGKX1822EK2SRWWB2MFXTEDN

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

M-11701303700659401223
M-11701403700659401179