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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

Nima Ecoform Pluma Skikt 45x45 cm — Class I MDR by Nimacare AB

MD Atlas
Nimacare AB

EUDAMED last updated this device on Apr 2, 2026

Nima Ecoform Pluma Skikt 45x45 cm

735005286ECOPS7P

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Nimacare AB
UDI-DI code: 07333376004376
Reference / catalog number: ECOPS4545

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Manufacturer information

Organization name: Nimacare AB
SRN: SE-MF-000050989
Manufacturer status: Active

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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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
The device must be used in accordance with the instructions for use. Incorrect use or positioning may increase the risk of pressure injury

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement	Apr 2, 2026	Still on market

Device identification

Trade name: Nima Ecoform Pluma Skikt 45x45 cm
UDI-DI code: 07333376004376
Basic UDI-DI: 735005286ECOPS7P
Reference / catalog number: ECOPS4545
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: Anatomical wheel chair cusion with a visco foam base. Gel inlay in the back and soft foam on top
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 45 MU10
45 MU10

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.

V08030102NON-ACTIVE ANTI-DECUBITUS MEDICAL CUSHIONS

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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