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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

B37.XL.7 — Class I MDR by Polstar Mateusz…

MD Atlas
Polstar Mateusz Ordyszewski

EUDAMED last updated this device on Jan 30, 2026

B37.XL.7

59049331bodydlasenioraKL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Polstar Mateusz Ordyszewski
UDI-DI code: 05904933157624
Reference / catalog number: B37.XL.7

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Manufacturer information

Organization name: Polstar Mateusz Ordyszewski
SRN: PL-MF-000036129
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 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: 05904933157624
Basic UDI-DI: 59049331bodydlasenioraKL
Reference / catalog number: B37.XL.7
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: Body dla seniora - krótki rękaw, zamek z przodu, długie nogawki, bez zamka w kroku ze ściągaczami - z wkładką nieprzemakalną z tyłu - Specjalistyczny ubiór dla osób z obniżoną sprawnością umysłową spowodowaną np. chorobami neurodegeneracyjnymi, w tym chorobą Alzheimera.Konstrukcja wyrobu zapobiega niekontrolowanemu zdejmowaniu body przez użytkownika i ogranicza jego dostęp do pieluchy czy pieluchomajtek. Wyrób ułatwia opiekunowi przeprowadzanie zabiegów pielęgnacyjnych bez zdejmowania body.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: XL
Czarny

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification

EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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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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.