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AngelAid

by Well Lands Enterprise Co., Ltd. 236 variants

Ref 20-641HR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471989783PositioningKitYK Basic UDI-DI 04719897839506UDI-DIDate20 Oct 2026RegisteredStatusActive

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  • Withdrawn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
AngelAid Trendelenburg Positioning Kit (Full Set)
Model / Reference
20-641HR
Primary DI / UDI-DI
04719897839506
Basic UDI-DI
471989783PositioningKitYK
EMDN Code
V080302 Patient positioning medical cushions
Device Class
Class I
Medical Purpose
One Basic UDI-DI covers all five kit types: same intended purpose (surgical patient positioning), same risk class, same foam-pad and strap design, same production site. Kit type, content and size are expressed at UDI-DI level.

Manufacturer details

EUDAMED SRN
TW-PR-000059668

Other devices from Well Lands Enterprise

See all devices from Well Lands Enterprise →

Properties

Other properties (1)

  • Sterile: No