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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

W.D.LJbez.5p — IVDR Class C IVDR by "BIOMED-LUBLIN"…

MD Atlas
"BIOMED-LUBLIN" Wytwórnia Surowic i Szczepionek Spółka Akcyjna

EUDAMED last updated this device on Jun 3, 2022

W.D.LJbez.5p

5907799163LJQP

On the marketIVDR Class C

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: "BIOMED-LUBLIN" Wytwórnia Surowic i Szczepionek Spółka Akcyjna
UDI-DI code: 05907799163013
Reference / catalog number: W.D.LJbez.5p

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View device family (Basic UDI)

Manufacturer information

Organization name: "BIOMED-LUBLIN" Wytwórnia Surowic i Szczepionek Spółka Akcyjna
SRN: PL-MF-000024087
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	May 26, 2022	May 26, 2026

Device identification

Trade name: not provided
UDI-DI code: 05907799163013
Basic UDI-DI: 5907799163LJQP
Reference / catalog number: W.D.LJbez.5p
Issuing entity: GS1

Classification

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

Device details

Quantity: 5
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)05907799163013

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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.

W0104010206MEDIA IN TUBES (SOLID & LIQUID)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

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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.