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Nylon

by Assut Medical Sàrl 194 variants

Ref 5533FModel Sterile synthetic non-absorbable surgical suture material

Nylon (5533F) is a Class III device made by Assut Medical Sàrl, registered in EUDAMED on 8 Jul 2026 (Basic UDI-DI B-07613406050246), active as of 24 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07613406050246 Basic UDI-DI Date8 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Nylon/Polyamide
Model / reference
Sterile synthetic non-absorbable surgical suture material, 5533F
Primary DI / UDI-DI
07613406050246, 07613406050253
Basic UDI-DI
B-07613406050246, B-07613406050253
EMDN code
H010201010101 Polyamide monofilament with needle
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CH-MF-000009358
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Similar devices in this category

Other devices filed under POLYAMIDE MONOFILAMENT WITH NEEDLE.

Other devices from Assut Medical Sàrl

See all devices from Assut Medical Sàrl →

Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)