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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

24-5253-P — Class I MDR by B.I.M.A. PLASTTEKNIK AB

MD Atlas
B.I.M.A. PLASTTEKNIK AB

EUDAMED last updated this device on May 27, 2026

24-5253-P

73400473(C)24-SERIESWU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: B.I.M.A. PLASTTEKNIK AB
UDI-DI code: 07340047336476
Reference / catalog number: 24-5253-P

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View device family (Basic UDI)

Manufacturer information

Organization name: B.I.M.A. PLASTTEKNIK AB
SRN: SE-MF-000001678
Manufacturer status: Active

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05-5745-P73400473(C)05-SERIESVZOn the market 05-6050-P73400473(C)05-SERIESVZOn the market 05-5740-K73400473(C)05-SERIESVZOn the market 05-6045-K73400473(C)05-SERIESVZOn the market 05-5050-K73400473(C)05-SERIESVZOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement	Jan 1, 1990	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07340047336476
Basic UDI-DI: 73400473(C)24-SERIESWU
Reference / catalog number: 24-5253-P
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: Tryckfördelande sittdyna som ger utpräglat stöd för låren samt avlastar sittbensknölar och svanskota. För brukare som sitter större delen av dagen, kan inte aktivt ändra läge/position i sittandet och har medelhög risk för trycksår. Brukaren behöver stöd/god positionering för att bibehålla ett funktionellt sittande.
Additional information URL: https://bimasweden.se/produkter/bima-combi/
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.

V080399MEDICAL CUSHIONS - 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.