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Filapron™ Polyglecaprone 25 Suture

by Meril Endo Surgery Pvt. Ltd. 92 variants

Ref MEC/BRC/013

Active European Union

CE MDR

Valid until

19 Feb 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberG70 105557 0008 Date30 Jun 2026IssuedStatusActive expires 19 Feb 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

Italy
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 1 country, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Italy since 18 Mar 2016

Last checked 24 Oct 2026.

Specification

EUDAMED

Device Name
FILAPRON™/ASPIRON™ Absorbable Poly (Glycolide-Co-Caprolactone) Surgical Suture
Model / Reference
MEC/BRC/013
Primary DI / UDI-DI
18906070904561, 18904255221892, 18906070904868, 18906070904769, 18904255205212, 18906070901133, 18904255221786, 18906070904660, 18904255221816, 18904255221755, 18906070907258, 18904255208640, 18904255207636, 18904255219608, 18906070904516, 18904255208619, 18904255221441, 18906070904622, 18904255232607, 18904255230610, 18906070904493, 18906070904646, 18904255228969, 18904255230924, 18904255205236, 18906070907159, 18904255221847, 18904255204062, 18904255221878, 18904255204840, 18904255229003, 18904255228990, 18904255208596, 18904255208671, 18906070904639, 18906070904851, 18904255232614, 18906070904691, 18904255230870, 18904255221779, 18906070904677, 18904255230696, 18906070904592, 18904255206974, 18904255230597, 18906070904882, 18904255230306, 18906070904813, 18904255230047, 18904255230054
Basic UDI-DI
89042552MES_PCL05VW
EMDN Code
H010101010301, H010101010302
Device Class
Class III
EU market of registration
Italy

Manufacturer details

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

Other devices from Meril Endo Surgery Pvt. Ltd.

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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