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Combo Red/Blue Articulating Paper

by Rayson Healthcare, Inc DBA Raydenco, Inc.

Ref 20 10 7003

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 Number0817807comboKX Basic UDI-DI 00817807000337UDI-DIDate22 Jul 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  • Withdrawn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
Thin Red/Blue Articulating Paper
Model / Reference
20 10 7003
Primary DI / UDI-DI
00817807000337
Basic UDI-DI
0817807comboKX
Direct Marketing DI
00817807000337
EMDN Code
Q01020201 Articulation papers
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
US-MF-000052071
Authorised representative
Obelis s.a. BE-AR-000000106

From the manufacturer

Manufacturer's product page: Articulating Paper

Other devices from Rayson Healthcare, Inc DBA Raydenco, Inc.

See all devices from Rayson Healthcare, Inc DBA Raydenco, Inc. →

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