Skip to content

Protecta

by Medstrom LTD

Ref 05060467210171Model 4

Protecta (05060467210171) is a Class I device made by Medstrom LTD, registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 5060467215060467210171R5), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5060467215060467210171R5 Basic UDI-DI 05060467210171UDI-DIDate2 Nov 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Protecta
Model / reference
4, 05060467210171
Primary DI / UDI-DI
05060467210171
Basic UDI-DI
5060467215060467210171R5
EMDN code
V080702 Non active anti-decubitus medical mattresses
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
UK-MF-000045032
Authorised representative
Freyr Regulatory GmbH DE-AR-000047121

Similar devices in this category

Other devices filed under NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES.

Other devices from Medstrom LTD

See all devices from Medstrom LTD →

Properties

Other properties (14, all answered No)