Skip to content

Spryly Laze Folding Backrest

by Spryly Limited

Ref SPRY-003-TPEModel SPRY-003-TPE SPRY-003-LIN SPRY-003-ED1 SPRY-003-ED2 SPRY-003-ED3 SPRY-003-ED4 SPRY-003-ED5

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50700039690SPRY-003UN Basic UDI-DI 05070003969067UDI-DIDate20 Nov 2025RegisteredStatusActive

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  • Withdrawn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
Spryly Laze Folding Backrest
Model / Reference
SPRY-003-TPE SPRY-003-LIN SPRY-003-ED1 SPRY-003-ED2 SPRY-003-ED3 SPRY-003-ED4 SPRY-003-ED5, SPRY-003-TPE
Primary DI / UDI-DI
05070003969067
Basic UDI-DI
50700039690SPRY-003UN
EMDN Code
Y121821 Retractors, backrests, brackets and supports
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
UK-MF-000050204
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Spryly Limited

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