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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

51030241 — Class I MDR by Orkla Wound Care AB

MD Atlas
Orkla Wound Care AB

EUDAMED last updated this device on Apr 17, 2026

51030241

73402101150042

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Orkla Wound Care AB
UDI-DI code: 07310610025403
Reference / catalog number: 51030241

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View device family (Basic UDI)

Manufacturer information

Organization name: Orkla Wound Care AB
SRN: SE-MF-000021041
Manufacturer status: Active

Related devices

90730227340210071004DOn the market 90730307340210071004DOn the market 90730497340210071004DOn the market 90730147340210071004DOn the market 5101101873402101150042On 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

No critical warnings reported for this device.

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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: 07310610025403
Basic UDI-DI: 73402101150042
Reference / catalog number: 51030241
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: —
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

UDI-DI DataMatrix

Encoded

(01)07310610025403

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

M0303010203ELASTIC FIXING BANDAGES, SELF-ADHESIVE, EXTENSIBLE IN TWO DIRECTIONS

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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