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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

068 — Class I MDR by Medizintechnik St.…

MD Atlas
Medizintechnik St. Egidien GmbH

EUDAMED last updated this device on Oct 1, 2024

068

426073068N5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medizintechnik St. Egidien GmbH
UDI-DI code: 04260739620023
Reference / catalog number: 068

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Manufacturer information

Organization name: Medizintechnik St. Egidien GmbH
SRN: DE-MF-000009064
Manufacturer status: Active

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074426073074MYOn the market 075426073962075B8On the market 075426073075N2On the market 054426073962054AYOn the market 083426073083MZOn 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
safety issue

Market distribution

Primary placement in Austria; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04260739620023
Basic UDI-DI: 426073068N5
Reference / catalog number: 068
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: Traumaarm zur Nutzung an einem Siemens-Röntgensystem
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039080VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL INSTRUMENTS - HARDWARE ACCESSORIES

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
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Software identification