ErgoPro entlordosierend (XXXL/M)

by spektramed GmbH

Ref 100024316Model ErgoPro entlordosierend

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number425055662314041BW Basic UDI-DI 04250556605235UDI-DI	Date10 Dec 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Withdrawn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: ErgoPro entlordosierend
Model / Reference: ErgoPro entlordosierend, 100024316

Primary DI / UDI-DI: 04250556605235
Basic UDI-DI: 425055662314041BW
Direct Marketing DI: 04250556604641
EMDN Code: Y060309 Thoracolumbosacral spine orthoses

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000005711

Other devices from spektramed GmbH

Ergo X-Large

Class I
ErgoPro entlordosierend (M/L)

Class I
ErgoSpine mit Mobilisierungsfunktion mit Adapter - kurz/XXL

Class I
ErgoSpine Pro ohne Mobilisierungsfunktion mit Adapter - lang/XXXL

Class I
Ergo XXX-Large

Class I
ErgoPro lordosierend (M/S)

Class I

See all devices from spektramed GmbH →

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