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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

OnctoDose — Class IIb MDR by ConnCons GmbH

MD Atlas
ConnCons GmbH

EUDAMED last updated this device on May 20, 2026

OnctoDose

426248185DOSECK

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ConnCons GmbH
UDI-DI code: 04262481850048
Reference / catalog number: DS-AP-001-C

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Manufacturer information

Organization name: ConnCons GmbH
SRN: DE-MF-000043807
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW999
CONTRAINDICATION: Premature births are contraindicated as a patient group.
CW999
WARNING: Adverse effects resulting from incorrect drug dosing (any reason) can lead to the need for dose reduction, delayed treatment or the discontinuation of treatment. WARNING: Excessive use of the file interface can negatively affect the entire system performance.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	May 26, 2026	Still on market

Device identification

Trade name: OnctoDose
UDI-DI code: 04262481850048
Basic UDI-DI: 426248185DOSECK
Reference / catalog number: DS-AP-001-C
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Software intended to assist in the calculation of patient-specific indices and medication dose during antineoplastic therapy. The calculation is based on the input data provided by the user.
Additional information URL: https://www.connected-consumables.com/products-onctodose
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12040292GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - 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

OnctoDose426248185DOSECKOn the market OnctoDose426248185DOSECKOn the market OnctoDose426248185DOSECKOn the market OnctoDose426248185DOSECKOn 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.