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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

MSW — Class I MDR by JJW Spółka Jawna J.…

MD Atlas
JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin

EUDAMED last updated this device on Jan 12, 2024

MSW

5901050MDSilverwoolE6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin
UDI-DI code: 05901050902526
Reference / catalog number: MSW

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View device family (Basic UDI)

Manufacturer information

Organization name: JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin
SRN: PL-MF-000009541
Manufacturer status: Active

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 Poland; available across 1 country total.

Placed on the market in Poland; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05901050902526
Basic UDI-DI: 5901050MDSilverwoolE6
Reference / catalog number: MSW
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: Socks MEDIC DEO SILVERWOOL grey, EU size 35-37
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.

Y0999PERSONAL CARE AIDS - OTHER

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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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.