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"Filaprop™ Non-absorbable Polypropylene Surgical Suture U.S.P "

by Meril Endo Surgery Pvt. Ltd. 329 variants

Ref ME/BRC/006

Active European Union

CE MDR

Valid until

4 May 2028

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 0009 Date30 Jun 2026IssuedStatusActive expires 4 May 2028

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  • Withdrawn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
Filaprop™ Non-absorbable Polypropylene Surgical Suture U.S.P
Model / Reference
ME/BRC/006
Primary DI / UDI-DI
18904255206202
Basic UDI-DI
89042552MES_PPL06YT
EMDN Code
H010201010401, H010201010402
Device Class
Class III
EU market of registration
Bulgaria

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