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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

K5038 — IVDR Class A IVDR by Nordic Biomarker AB

MD Atlas
Nordic Biomarker AB

EUDAMED last updated this device on Apr 10, 2026

K5038

7350060320016L

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Nordic Biomarker AB
UDI-DI code: 27350060320042
Reference / catalog number: K5038

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Manufacturer information

Organization name: Nordic Biomarker AB
SRN: SE-MF-000022201
Manufacturer status: Active

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SC106K73500603201773On the market SC107K73500603201875On the market SC105K7350060320297AOn the market 1200117350060320026NOn the market AR037K73500603203473On 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: 27350060320042
Basic UDI-DI: 7350060320016L
Reference / catalog number: K5038
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: 6 x 100 mL
Additional information URL: https://www.nordicbiomarker.com/
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.

W0103020903BUFFERS (HAEMOSTASIS)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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