Skip to content

Mericron XL™ Polyester Surgical Suture U.S.P.

by Meril Endo Surgery Pvt. Ltd. 78 variants

Ref ME/BRC/025

Active European Union

CE MDR

Valid until

15 Jan 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

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/MDR NumberG70 105557 0012 Date30 Jun 2026IssuedStatusActive expires 15 Jan 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Mericron XL™/Aspiron™ Non absorbable Poly (Ethylene Terephthalate) Surgical Suture U.S.P.
Model / Reference
ME/BRC/025
Primary DI / UDI-DI
18904255224565
Basic UDI-DI
89042552MES_PES08XM
EMDN Code
H010201020201, H010201020203
Device Class
Class III
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
IN-MF-000010999
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Meril Endo Surgery Pvt. Ltd.

See all devices from Meril Endo Surgery Pvt. Ltd. →

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