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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

Kemokur v3.0 — Class IIb MDR by CGI Suomi Oy

MD Atlas
CGI Suomi Oy

EUDAMED last updated this device on Dec 12, 2025

Kemokur v3.0

643007895KEMOKUR03MJ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CGI Suomi Oy
UDI-DI code: 06430078950046
Reference / catalog number: Kemokur v3.0

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Manufacturer information

Organization name: CGI Suomi Oy
SRN: FI-MF-000012661
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement	Dec 11, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 06430078950046
Basic UDI-DI: 643007895KEMOKUR03MJ
Reference / catalog number: Kemokur v3.0
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: The Kemokur application is intended as a tool to assist in managing medical treatments that require special planning for patients of all ages in a hospital setting. Treatments used according to the intended purpose include, for example, cytotoxic-based, biological, and similar therapies used in the treatment of cancer and autoimmune diseases, as well as their supportive medications. Kemokur manages patient-specific medication and pharmacy orders and documents the treatment processes. The implementation of treatment and the approval of administered doses always belongs to the physician responsible for the patient's care. The system is not intended to plan or make decisions related to a patient's treatment without the assessment of the treating physician.
Additional information URL: No additional information URL provided by the manufacturer.
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

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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.