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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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Organization name
UDI-DI code
Reference / catalog number

0100025 — Class IIb MDR by LMT Medical Systems GmbH

MD Atlas
LMT Medical Systems GmbH

EUDAMED last updated this device on May 18, 2026

0100025

426048661nomag3K

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LMT Medical Systems GmbH
UDI-DI code: 04260486610575
Reference / catalog number: 0100025

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Manufacturer information

Organization name: LMT Medical Systems GmbH
SRN: DE-MF-000005238
Manufacturer status: Active

Critical warnings

8 warnings recorded — scroll inside the panel to see all entries.

CW999
MR conditional <= 3T
CW999
<= 28T/m (<=2800 gauss/cm) Equipment operation may be impacted Do not exceed 3T (30 000 gauss)
CW999
Use an oxygen monitor when oxygen is administered
CW999
Warning! Never leave baby unattended, when flap or handport are open. Always lock after closing! Do not block or obstruct air inlet. Risk of patient injury (burns)!
CW016
Patientenbett
CW010
EUDAMED did not publish a description for this code.
CW999
The nomag® IC Advanced with the related trolley is for intrahospital use only and not for use in ambulance cars or helicopters.
CW999
The usage on patients > 4.5 kg or > 55 cm is not indicated.

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Market distribution

Primary placement in Norway; available across 1 country total.

Country	On market since	Until
NorwayPrimary placement	Aug 6, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260486610575
Basic UDI-DI: 426048661nomag3K
Reference / catalog number: 0100025
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z1208040302MOBILE NEONATAL INCUBATORS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

Certificate health across this manufacturer's portfolio.

G10 087909 0012Issued
Quality management systemNotified body: 0123Expiry: Jul 26, 2026