AltiPress40 Med REG lgth beige kit

by urgo ltd EUDAMED

Active European Union

Ref 558237

Regulatory status

as of 26 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number5021300ALTIPRESSXD Basic UDI-DI	Date11 May 2026Registered	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name: Altipress
Model / Reference: 558237

Primary DI / UDI-DI: 05060064274088

Market of Registration: Ireland

Manufacturer details

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

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