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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

QDOZ-0004-000 — Class I MDR by Lubelskie Zakłady…

MD Atlas
Lubelskie Zakłady Farmaceutyczne "POLFA" Spółka Akcyjna

EUDAMED last updated this device on Jul 28, 2025

QDOZ-0004-000

5906188Dozowniki-kImPY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lubelskie Zakłady Farmaceutyczne "POLFA" Spółka Akcyjna
UDI-DI code: 05906188005361
Reference / catalog number: QDOZ-0004-000

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View device family (Basic UDI)

Manufacturer information

Organization name: Lubelskie Zakłady Farmaceutyczne "POLFA" Spółka Akcyjna
SRN: PL-MF-000015608
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.

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

Device identification

Trade name: not provided
UDI-DI code: 05906188005361
Basic UDI-DI: 5906188Dozowniki-kImPY
Reference / catalog number: QDOZ-0004-000
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: 1100
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 0–5 MU03

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05906188005361

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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.

V0380DEVICES WITH MEASURING FUNCTIONS - ACCESSORIES

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

Certificate health across this manufacturer's portfolio.

TNP/MDR/0024/0052/2024Issued
Quality assuranceNotified body: 2274Expiry: Sep 5, 2027