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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

I20-R0115 — IVDD — General IVDD by PZ CORMAY Spółka Akcyjna

MD Atlas
PZ CORMAY Spółka Akcyjna

EUDAMED last updated this device on Oct 14, 2025

I20-R0115

B-05907514601349

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: PZ CORMAY Spółka Akcyjna
UDI-DI code: 05907514601349
Reference / catalog number: I20-R0115

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View device family (Basic UDI)

Manufacturer information

Organization name: PZ CORMAY Spółka Akcyjna
SRN: PL-MF-000023053
Manufacturer status: Active

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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: 05907514601349
Basic UDI-DI: B-05907514601349
Reference / catalog number: I20-R0115
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Control Material (High) 1 x 1 Control Material (Low) 1 x 1 Caibrator (High) 1 x 1 Calibrator (Low) 1 x 1 MB 1 x 1,8 RB 1 x 3 RA 1 x 3,5
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)05907514601349

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EMDN nomenclature code(s)

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

W0102030116SQUAMOUS CELL CARCINOMA ANTIGEN

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

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.