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P.G.A. ARAGÓ Ácido poliglicólico recubierto

by Laboratorio Aragó S.L. EUDAMED

Active European Union

Ref 38240

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8427599DTTF0147C Basic UDI-DIDate29 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2025 DR 0061 Issued

    Technical documentation EU MDR

    Notified body
    Notified body 0318
    Issued
    18 Sep 2025
    Expires
    17 Jul 2030

Specification

EUDAMED

Device Name
Sutura de P.G.A. (ácido poliglicólico)
Model / Reference
38240
Primary DI / UDI-DI
08427599001645
Basic UDI-DI
8427599DTTF0147C
EMDN Code
H010101020101 Polyglycolic acid multifilament with needle for open surgery
Device Class
Class III
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