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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

PS013000 — Class I MDR by Caretec i Forserum AB

MD Atlas
Caretec i Forserum AB

EUDAMED last updated this device on Apr 27, 2026

PS013000

7332894PS013000LK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Caretec i Forserum AB
UDI-DI code: 07332894200178
Reference / catalog number: PS013000

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View device family (Basic UDI)

Manufacturer information

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

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800000733289420530EEOn the market 80000073328948000004QOn the market 41060073328944106004DOn the market 10554733289410554EHOn the market 71087173328947108716MOn 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 15, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07332894200178
Basic UDI-DI: 7332894PS013000LK
Reference / catalog number: PS013000
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: Avsedd användning. Princess sängryggstöd är framtagen och avsedd att användas i områdena AE3, AE4 samt AE5 enligt IEC 60601-2-52. Det motsvarar hemmiljö eller institutionell miljö, ex. vårdhem eller äldreboende.
Additional information URL: https://www.caretec.se/hemsjukvard/sangryggstod/princess-sangryggstod
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.

Y121821RETRACTORS, BACKRESTS, BRACKETS AND SUPPORTS

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.