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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

Shitfak — Class I MDR by CVN medical Oy

MD Atlas
CVN medical Oy

EUDAMED last updated this device on Aug 14, 2025

Shitfak

64298101440642981014458K5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CVN medical Oy
UDI-DI code: 06429810144584
Reference / catalog number: H500-9010V

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Manufacturer information

Organization name: CVN medical Oy
SRN: FI-MF-000032554
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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: Shitfak
UDI-DI code: 06429810144584
Basic UDI-DI: 64298101440642981014458K5
Reference / catalog number: H500-9010V
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Shooter’s Individual Tactical First Aid Kit. First aid kit for emergency treatment of trauma.
Additional information URL: https://www.cvn.fi/
Clinical sizes: 280–300 MU29

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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.