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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

410100 — Class I MDR by Caretec i Forserum AB

MD Atlas
Caretec i Forserum AB

EUDAMED last updated this device on Apr 23, 2026

410100

73328944101003L

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Caretec i Forserum AB
UDI-DI code: 07332894200062
Reference / catalog number: 410100

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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 16, 1998	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07332894200062
Basic UDI-DI: 73328944101003L
Reference / catalog number: 410100
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: Sängbord PRO är ett klassiskt sängbord för sjukhus och andra vårdmiljöer. Tydlig design och tåliga material gör bordet lätt att hantera och underhålla. Lådorna är hygieniskt utformade och kan maskindiskas. Bordet kan kompletteras med olika tillbehör.
Additional information URL: https://www.caretec.se/sjukvard/sangbord-sjukvard/pro
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)07332894200062

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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.