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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

90-8050-K — 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

90-8050-K

7340047390-SERIES3X

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: 07340047354197
Reference / catalog number: 90-8050-K

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Manufacturer information

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

Related devices

10-3535-PB-07340047300811On the market 10-3535-K7340047310-SERIESW4On the market 40-5247-K73400473(C)40-SERIESVWOn the market 40-5243-P73400473(C)40-SERIESVWOn the market 40-5555-P73400473(C)40-SERIESVWOn 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: 07340047354197
Basic UDI-DI: 7340047390-SERIES3X
Reference / catalog number: 90-8050-K
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: Stabil och tryckavlastande rullstolsdyna, anpassad för stora och tunga personer som är beroende av rullstol för sina förflyttningar och har svårt att variera sittandet. Bima XXL är förebyggande mot sår
Additional information URL: https://bimasweden.se/produkter/bima-xxl/
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.