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Ref, Allegro 2 Reformer w Risers

by Balanced Body Inc

Part of a family of 152 devices: see the family page

Ref 12505

Ref, Allegro 2 Reformer w Risers (12505) is a Class I device made by Balanced Body Inc, registered in EUDAMED on 7 Feb 2025 (Basic UDI-DI 0810052148000LS), 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 Number0810052148000LS Basic UDI-DI 00810052140810UDI-DIDate7 Feb 2025RegisteredStatusActive

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  • Withdrawn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
Reformer-Trapeze Combination (RTC)
Model / reference
12505
Primary DI / UDI-DI
00810052140810
Basic UDI-DI
0810052148000LS
EMDN code
Z12069099 Various physiotherapy and rehabilitation instruments - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000045340
Authorised representative
Emergo Europe B.V. NL-AR-000000116

From the manufacturer

Manufacturer's product page: How to Choose a Reformer

Similar devices in this category

Other devices filed under VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER.

Other devices from Balanced Body Inc

See all devices from Balanced Body Inc →

Properties

Other properties (14, all answered No)