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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 600 Tät Mesh 33x33 cm — Class I MDR by Nimacare AB

MD Atlas
Nimacare AB

EUDAMED last updated this device on May 19, 2026

Nima 600 Tät Mesh 33x33 cm

735005286600TMS6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Nimacare AB
UDI-DI code: 07333376013316
Reference / catalog number: 600TM3333

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Manufacturer information

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

Related devices

Nima 600 MESH 30x30 cm735005286600MESHM5On the market Nima 600 MESH 30x33 cm735005286600MESHM5On the market Nima 600 MESH 33x30 cm735005286600MESHM5On the market Nima 600 MESH 33x33 cm735005286600MESHM5On the market Nima 600 MESH 35x30 cm735005286600MESHM5On 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		Still on market

Device identification

Trade name: Nima 600 Tät Mesh 33x33 cm
UDI-DI code: 07333376013316
Basic UDI-DI: 735005286600TMS6
Reference / catalog number: 600TM3333
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: Cushion made up of several layers of foam with mesh fabric cover
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 33 MU10
33 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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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.