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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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NeoNatalie Resuscitator — 4 UDI-DI variants, MDR (Laerdal Medical AS)

MD Atlas
Laerdal Medical AS

Data from EUDAMED, last updated May 30, 2026

NeoNatalie Resuscitator

0704543209947TA

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: Laerdal Medical AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0704543209947TA
Device name: NeoNatalie Resuscitator
Device model: NeoNatalie Resuscitator
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Laerdal Medical AS
SRN: NO-MF-000000012
Country: Norway
Email: PRRC@laerdal.com
Phone: +47 51511700

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GGETMS1AAWDWP0B1XZE3EHA1

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

LGH-84604007045432092004
84604007045432051209
NeoNatalie Resuscitator Oxygen kit07045432051230
NeoNatalie Resuscitator Oxygen kit07045432092011