Ode Outdoor Base

by Timoteos Oy 4 variants

Ref 66111M

Active European Union

CE MDR

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number643001637ODED5 Basic UDI-DI 06430016370196UDI-DI	Date25 Oct 2021Registered	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Withdrawn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/MDR Active

Specification

EUDAMED

Device Name: Ode Seating System
Model / Reference: 66111M

Primary DI / UDI-DI: 06430016370196
Basic UDI-DI: 643001637ODED5
Direct Marketing DI: 06430016370196
EMDN Code: Y180918 Multifunctional chairs

Device Class: Class I
EU market of registration: Finland

Manufacturer details

EUDAMED SRN: FI-MF-000011749

Other devices from Timoteos Oy

Ella Stander

Class I
Ode Indoor Base

Class I
Ode Outdoor Base

Class I
Ode Seat

Class I
Ella Stander

Class I
Ella Stander

Class I

See all devices from Timoteos Oy →

Properties

Other properties (13)

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