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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

L905160502 — Class I MDR by Aktiebolaget…

MD Atlas
Aktiebolaget Elektronik-Konstruktion Innovation

EUDAMED last updated this device on May 26, 2026

L905160502

7350118260058K

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aktiebolaget Elektronik-Konstruktion Innovation
UDI-DI code: 07350118260050
Reference / catalog number: L905160502

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View device family (Basic UDI)

Manufacturer information

Organization name: Aktiebolaget Elektronik-Konstruktion Innovation
SRN: SE-MF-000008551
Manufacturer status: Active

Related devices

L9051404007350118260088ROn the market L9050350007350118260018BOn the market L9051500007350118260038FOn the market L9051550007350118260048HOn the market L9051407057350118260068MOn the market

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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07350118260050
Basic UDI-DI: 7350118260058K
Reference / catalog number: L905160502
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Blood donor bag tube sealer
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.

B0180BLOOD BAGS AND KITS - ACCESSORIES

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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