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Poliamid

by Metaloplast podjetje za proizvodno, trgovsko in storitveno dejavnost d.o.o. Kobarid

Ref N162RModel Polyamide

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number383004001NY1AY Basic UDI-DI 03830040010502UDI-DIDate23 Oct 2024RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Polyamide suture
Model / Reference
Polyamide, N162R
Primary DI / UDI-DI
03830040010502
Basic UDI-DI
383004001NY1AY
EMDN Code
H010201010101 Polyamide monofilament with needle
Device Class
Class IIb
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000004241

Other devices from Metaloplast podjetje za proizvodno, trgovsko in storitveno dejavnost d.o.o. Kobarid

Properties

  • Sterile
  • Implantable
  • Sutures

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