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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

0100015 — Class IIb MDR by LMT Medical Systems GmbH

MD Atlas
LMT Medical Systems GmbH

EUDAMED last updated this device on May 6, 2026

0100015

426048661nomag3K

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LMT Medical Systems GmbH
UDI-DI code: 04260486610568
Reference / catalog number: 0100015

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Manufacturer information

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

Critical warnings

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

CW016
EUDAMED did not publish a description for this code.
CW011
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)!
CW999
Max. Patient weight 4,5kg
CW999
MR conditional ≤ 1.5 T
CW999
≤ 28T/m (≤2800 gauss/cm) Equipment operation may be impacted Do not exceed 1,5T (15.000 gauss)
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Austria; available across 1 country total.

Country	On market since	Until
AustriaPrimary placement	Apr 30, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260486610568
Basic UDI-DI: 426048661nomag3K
Reference / catalog number: 0100015
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.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.