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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

172210 — Class I MDR by Ideal Partner Spółka z…

MD Atlas
Ideal Partner Spółka z ograniczoną odpowiedzialnością Spółka komandytowa

EUDAMED last updated this device on May 23, 2025

172210

590115762CAPSAT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ideal Partner Spółka z ograniczoną odpowiedzialnością Spółka komandytowa
UDI-DI code: 05901157625427
Reference / catalog number: 172210

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Manufacturer information

Organization name: Ideal Partner Spółka z ograniczoną odpowiedzialnością Spółka komandytowa
SRN: PL-MF-000047903
Manufacturer status: Active

Related devices

184110590115762CAPSATOn the market 184210590115762CAPSATOn the market 172110590115762CAPSATOn the market 182210590115762CAPSATOn the market 182110590115762CAPSATOn 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

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: 05901157625427
Basic UDI-DI: 590115762CAPSAT
Reference / catalog number: 172210
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: 100
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

EMDN nomenclature code(s)

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

T0207CAPS AND HEADWEAR (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE)

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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