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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

POPE5 — Class I MDR by MIRACLE ROBERT…

MD Atlas
MIRACLE ROBERT BIEGAŃSKI MAŁGORZATA BAUER SPÓŁKA JAWNA

EUDAMED last updated this device on Aug 13, 2025

POPE5

59050686953POC5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MIRACLE ROBERT BIEGAŃSKI MAŁGORZATA BAUER SPÓŁKA JAWNA
UDI-DI code: 05905068695340
Reference / catalog number: POPE5

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View device family (Basic UDI)

Manufacturer information

Organization name: MIRACLE ROBERT BIEGAŃSKI MAŁGORZATA BAUER SPÓŁKA JAWNA
SRN: PL-MF-000040195
Manufacturer status: Active

Related devices

POAD259050686953POC5On the market POE359050686953POC5On the market POE4U59050686953POC5On the market POP159050686953POC5On the market POS359050686953POC5On the market

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.

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: 05905068695340
Basic UDI-DI: 59050686953POC5
Reference / catalog number: POPE5
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: 1
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)05905068695340

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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.

Y210699ELECTRONIC OPTICAL AIDS - OTHER

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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