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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

5320-4 — Class I MDR by Arcomed AG

MD Atlas
Arcomed AG

EUDAMED last updated this device on May 4, 2026

5320-4

764013713-MRI6U

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Arcomed AG
UDI-DI code: 07640137131814
Reference / catalog number: 5320-4

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Manufacturer information

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

Related devices

5310-5411764013713-UCB69On the market 5310-5412764013713-UCB69On the market 5310-5413764013713-UCB69On the market 5310-5414764013713-UCB69On the market 5310-5415764013713-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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07640137131814
Basic UDI-DI: 764013713-MRI6U
Reference / catalog number: 5320-4
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: UniQueMRIShield provides MRI shielding for arcomed infusion pumps
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

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Expiration date
Manufacturing date
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Software identification