Skip to content

Revitive Circulation Booster

by Actegy Limited 6 variants

Ref 5572AQModel 5572AQ-FR-BEN, 5572AQ-DE

Revitive Circulation Booster (5572AQ) is a medical device (EU MDD Class IIa; EMDN category muscle stimulators) made by Actegy Limited, registered in EUDAMED on 22 May 2026 (Basic UDI-DI B-05060217496404), active as of 23 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060217496404 Basic UDI-DI Date22 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Revitive ProHealth
Model / reference
5572AQ-FR-BEN, 5572AQ, 5572AQ-DE
Primary DI / UDI-DI
05060217496404, 05060217496213
Basic UDI-DI
B-05060217496404, B-05060217496213
EMDN code
Z120622 Muscle stimulators
Device class
Class IIa
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
France
Germany

Manufacturer details

EUDAMED SRN
GB-MF-000032543
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under MUSCLE STIMULATORS.

Other devices from Actegy Limited

See all devices from Actegy Limited →

Properties

Other properties (12, all answered No)