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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

ECG paper 110 mm x 40 m — Class I MDR by Hegard spółka z…

MD Atlas
Hegard spółka z ograniczoną odpowiedzialnością

EUDAMED last updated this device on Mar 9, 2026

ECG paper 110 mm x 40 m

59017923MDPREKGVZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Hegard spółka z ograniczoną odpowiedzialnością
UDI-DI code: 05901792311112
Reference / catalog number: MDP.055.110.040.19

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Manufacturer information

Organization name: Hegard spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000050050
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: ECG paper 110 mm x 40 m
UDI-DI code: 05901792311112
Basic UDI-DI: 59017923MDPREKGVZ
Reference / catalog number: MDP.055.110.040.19
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: 10
Additional product description: Technical paper in rolls used as a base for printing medical results in medical device printers. The product is intended for recording ECG test results.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 40 MU36
19 MU50
110 MU50

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.

Z1302DIAGNOSTIC REGISTRATION PAPERS

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.