Biofrost Active 3ml

by Viking Lab Oy

Ref BF2003

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-06430070090139 Basic UDI-DI 06430070090139UDI-DI	Date21 Jul 2023Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference: BF2003

Primary DI / UDI-DI: 06430070090139
Basic UDI-DI: B-06430070090139
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Finland

Manufacturer details

EUDAMED SRN: FI-MF-000005746

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Properties

Other properties (11)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No