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PAQ.144X100X350*31*SCH.AT6.MN 2914403

by Ab Medica Group, S.A.

Ref 2914403

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number84287631029PAPGRIDXF Basic UDI-DI 08428763009085UDI-DIDate10 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08428763009085 UDI-DI Date12 Nov 2025ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Papeles de registro médico LESSA EUDAMED
PAQ.144X100X350*31*SCH.AT6.MN GUDID
Generic Name
Electrocardiographic recording paper
Device Name
Papeles de registro médico
Model / Reference
2914403
Primary DI / UDI-DI
08428763009085
Basic UDI-DI
84287631029PAPGRIDXF
FDA Product Code
DSF
EMDN Code
Z1302 Diagnostic registration papers
GMDN Term
Electrocardiographic recording paper
Device Class
Class I
Regulation Number
870.2810
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Other devices from Ab Medica Group, S.A.

See all devices from Ab Medica Group, S.A. →

Properties

  • Single Use
  • Measuring Function
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (18)

  • 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
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No