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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

0800221 — Class IIa MDR by LMT Medical Systems GmbH

MD Atlas
LMT Medical Systems GmbH

EUDAMED last updated this device on May 22, 2026

0800221

426048661CoilsPK

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LMT Medical Systems GmbH
UDI-DI code: 04260486610582
Reference / catalog number: 0800221

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View device family (Basic UDI)

Manufacturer information

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

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW014
EUDAMED did not publish a description for this code.
CW999
Max Patient weight 4,5kg

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Nov 7, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260486610582
Basic UDI-DI: 426048661CoilsPK
Reference / catalog number: 0800221
Issuing entity: GS1

Classification

Risk category: Class IIa
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.

Z1105018001MAGNETIC RESONANCE (MR) RADIOFREQUENCY SURFACE COILS

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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Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

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