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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

MerryArm toalettarmstöd, 78 cm — Class I MDR by Swereco AB

MD Atlas
Swereco AB

EUDAMED last updated this device on May 12, 2026

MerryArm toalettarmstöd, 78 cm

7331427Y18C5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Swereco AB
UDI-DI code: 07331427090682
Reference / catalog number: 720624

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View device family (Basic UDI)

Manufacturer information

Organization name: Swereco AB
SRN: SE-MF-000033314
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

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: MerryArm toalettarmstöd, 78 cm
UDI-DI code: 07331427090682
Basic UDI-DI: 7331427Y18C5
Reference / catalog number: 720624
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: The MerryArm toilet armrest is used as an aid for sitting on or getting up from the toilet. The attachment for the toilet paper roll holder enables mounting of the holder on the toilet armrest
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07331427090682

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Y181809ARMRESTS

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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