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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

5310-5411 — Class I MDR by Arcomed AG

MD Atlas
Arcomed AG

EUDAMED last updated this device on Feb 5, 2026

5310-5411

764013713-UCB69

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Arcomed AG
UDI-DI code: 07640137131609
Reference / catalog number: 5310-5411

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Manufacturer information

Organization name: Arcomed AG
SRN: CH-MF-000035749
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 07640137131609
Basic UDI-DI: 764013713-UCB69
Reference / catalog number: 5310-5411
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: UniQueConcept is a data interface between arcomed infusion pumps and a network
Additional information URL: https://www.arcomed.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

5310-5412764013713-UCB69On the market 5310-5413764013713-UCB69On the market 5310-5414764013713-UCB69On the market 5310-5415764013713-UCB69On the market 5310-5416764013713-UCB69On the market

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.