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Polypropylene

by Gmd Group Medi̇kal Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 27 variants

Ref JE3SK60

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-08681677075076X5 Basic UDI-DI D-08681677075076X5UDI-DIDate13 Dec 2022RegisteredStatusActive

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

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Polypropylene (PP), 3-0, 60 mm, düz ters keskin iğne,mavi,emilmeyen, 75 cm sütür
Model / Reference
JE3SK60
Primary DI / UDI-DI
D-08681677075076X5
Basic UDI-DI
B-08681677075076X5
EMDN Code
H010201010401 Polypropylene monofilament with needle for open surgery
Device Class
Class III
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000030794

Other devices from Gmd Group Medi̇kal Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from Gmd Group Medi̇kal Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No