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P.G.A. ARAGÓ Ácido poliglicólico recubierto

by Laboratorio Aragó S.L. 548 variants

Ref 38498

Active European Union

CE MDR

Valid until

17 Jul 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS

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 Number8427599DTTF0147C Basic UDI-DI 08427599002970UDI-DIDate29 May 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2025 DR 0061 Active

    Technical documentation EU MDR

    Certifier
    CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS 0318
    Issued
    18 Sep 2025
    Expires
    17 Jul 2030

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Sutura de P.G.A. (ácido poliglicólico)
Model / Reference
38498
Primary DI / UDI-DI
08427599002970
Basic UDI-DI
8427599DTTF0147C
EMDN Code
H010101020101 Polyglycolic acid multifilament with needle for open surgery
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001958

Other devices from Laboratorio Aragó S.L.

See all devices from Laboratorio Aragó S.L. →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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