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Advabond

by Advanced MedTech Solutions Private Limited EUDAMED

Active European Union

Ref USP 5,4,3,2,1,0,2-0,3-0,4-0,5-0

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-89042724ADVABONDXAXV Basic UDI-DIDate9 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

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.

Specification

EUDAMED

Device Name
ADVABOND-Non-Absorbable Surgical Suture U.S.P. Braided Coated Polyester
Model / Reference
USP 5, 4, 3, 2, 1, 0, 2-0, 3-0, 4-0, 5-0
Primary DI / UDI-DI
D-89042724ADVABONDXAXV
Basic UDI-DI
B-89042724ADVABONDXAXV
EMDN Code
H010201020201, H010201020203
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IN-MF-000016196
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Advanced MedTech Solutions Private Limited

See all devices from Advanced MedTech Solutions Private Limited →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • 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