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Organization name
UDI-DI code
Reference / catalog number

OC,S,Uni,Dr_Goetz10BlueMix,39-42 — Class I MDR by Occulto GmbH

MD Atlas
Occulto GmbH

EUDAMED last updated this device on Apr 30, 2026

OC,S,Uni,Dr_Goetz10BlueMix,39-42

426061284GoetzN7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Occulto GmbH
UDI-DI code: 04260770471431
Reference / catalog number: OC,S,Uni,Dr_Goetz10BlueMix,39-42

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Manufacturer information

Organization name: Occulto GmbH
SRN: DE-MF-000053512
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Dec 20, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260770471431
Basic UDI-DI: 426061284GoetzN7
Reference / catalog number: OC,S,Uni,Dr_Goetz10BlueMix,39-42
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: 10
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 39–42 MU999

EMDN nomenclature code(s)

M030405COMPRESSION STOCKINGS

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
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Software identification

Related devices

This device is not currently linked to any other device.

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.