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Organization name
UDI-DI code
Reference / catalog number

Kemokur 1.5 — Class IIb MDD by CGI Suomi Oy

MD Atlas
CGI Suomi Oy

EUDAMED last updated this device on Dec 11, 2025

Kemokur 1.5

B-Kemokur1.57Y

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: CGI Suomi Oy
UDI-DI code: D-Kemokur1.57Y
Reference / catalog number: Kemokur 1.5

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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		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-Kemokur1.57Y
Basic UDI-DI: B-Kemokur1.57Y
Reference / catalog number: Kemokur 1.5
Issuing entity: EUDAMED

Classification

Risk category: Class IIb
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)

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

Certificate health across this manufacturer's portfolio.

CR-03-1156-859-24Supplemented
Quality management systemNotified body: 0537Expiry: Dec 9, 2029