AltiPress Lpck OpenToe XXL REG, bge

Ref 193701

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	Number5021300ALTIPRESSXD Basic UDI-DI 05060064275252UDI-DI	Date11 May 2026Registered	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Withdrawn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: Altipress
Model / Reference: 193701

Primary DI / UDI-DI: 05060064275252
Basic UDI-DI: 5021300ALTIPRESSXD
EMDN Code: M030405 Compression stockings

Device Class: Class I
EU market of registration: Ireland

Manufacturer details

EUDAMED SRN: GB-MF-000029696
Authorised representative: LABORATOIRES URGO FR-AR-000022224

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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