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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

410600 — Class I MDR by Caretec i Forserum AB

MD Atlas
Caretec i Forserum AB

EUDAMED last updated this device on Apr 23, 2026

410600

73328944106004D

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Caretec i Forserum AB
UDI-DI code: 07332894200086
Reference / catalog number: 410600

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View device family (Basic UDI)

Manufacturer information

Organization name: Caretec i Forserum AB
SRN: SE-MF-000036038
Manufacturer status: Active

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, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07332894200086
Basic UDI-DI: 73328944106004D
Reference / catalog number: 410600
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: Caretecs brickbord kan användas som läs, måltids eller arbetsbord. Bordet kan smidigt placeras över en säng eller stol. Skivan är vridbar åt båda sidor. Bordet är stabilt och solitt med bromsar på alla 4 hjul. Skivan är tillverkad i kompaktlaminat är steglöst höj och sänkbar med ett enkelt handgrepp.
Additional information URL: https://www.caretec.se/sjukvard/sangbord-sjukvard/caretec-brick
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)07332894200086

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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.

Y1803ASSISTIVE TABLES

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.