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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

0083/Version 1.7 — Class I MDD by Neo Q Quality in…

MD Atlas
Neo Q Quality in Imaging GmbH

EUDAMED last updated this device on Jun 7, 2023

0083/Version 1.7

B-4260710830083T4

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Neo Q Quality in Imaging GmbH
UDI-DI code: D-4260710830083T4
Reference / catalog number: 0083/Version 1.7

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Manufacturer information

Organization name: Neo Q Quality in Imaging GmbH
SRN: DE-MF-000015653
Manufacturer status: Inactive

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Feb 11, 2021	Still on market
Austria	Jul 1, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-4260710830083T4
Basic UDI-DI: B-4260710830083T4
Reference / catalog number: 0083/Version 1.7
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

This device is not currently linked to any other device.

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.