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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

3.10 — Class I MDD by alanta health group GmbH

MD Atlas
alanta health group GmbH

EUDAMED last updated this device on Sep 29, 2024

3.10

B-oncotraceLT

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: alanta health group GmbH
UDI-DI code: D-oncotraceLT
Reference / catalog number: 3.10

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Manufacturer information

Organization name: alanta health group GmbH
SRN: DE-MF-000034314
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: D-oncotraceLT
Basic UDI-DI: B-oncotraceLT
Reference / catalog number: 3.10
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: Therapieplanungs-, Therapiemanagement und Tumordokumentationssystem
Additional information URL: https://www.oncotrace.org/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z129092VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - MEDICAL DEVICE SOFTWARE

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.