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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

7-430 — IVDD — General IVDD by PZ CORMAY Spółka Akcyjna

MD Atlas
PZ CORMAY Spółka Akcyjna

EUDAMED last updated this device on Feb 16, 2026

7-430

B-05907514674305

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: 05907514674305
Reference / catalog number: 7-430

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View device family (Basic UDI)

Manufacturer information

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

Related devices

7-438B-05907514674381On the market 3-111590751463-1113POn the market 7-416B-05907514674169On the market 3-110590751463-1103MOn the market 7-412B-05907514674121On the market

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: 05907514674305
Basic UDI-DI: B-05907514674305
Reference / catalog number: 7-430
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: R1: 1 x 30 mL R2: 1 x 15 mL
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)05907514674305

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EMDN nomenclature code(s)

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

W0102070102FERRITIN

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.