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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

Indoor base in.basic — Class I MDR by MyWam Sp. z o.o.

MD Atlas
MyWam Sp. z o.o.

EUDAMED last updated this device on May 27, 2026

Indoor base in.basic

5901122279InBasic4P

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MyWam Sp. z o.o.
UDI-DI code: 05901122279358
Reference / catalog number: PJ

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View device family (Basic UDI)

Manufacturer information

Organization name: MyWam Sp. z o.o.
SRN: PL-MF-000019252
Manufacturer status: Active

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Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement	Mar 31, 2026	Still on market

Device identification

Trade name: Indoor base in.basic
UDI-DI code: 05901122279358
Basic UDI-DI: 5901122279InBasic4P
Reference / catalog number: PJ
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: The in.basic indoor base fits the Mouse and Mewa stroller seats.
Additional information URL: https://mywam.eu/produkt/podstawa-pokojowa-in-basic/
Clinical sizes: 40 kg
80–125 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05901122279358

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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.

Y122103PUSH WHEELCHAIRS

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.