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Mitsu FST™ - Absorbable Poly (Glycolide/L-Lactide) Surgical Suture U.S.P.

by Meril Endo Surgery Pvt. Ltd. 53 variants

Ref ME/BRC/019

Active European Union

CE MDR

Valid until

8 Oct 2029

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 0013 Date30 Jun 2026IssuedStatusActive expires 8 Oct 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

Bulgaria
  • 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  • Withdrawn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.

  • Bulgaria since 15 Mar 2016

Last checked 23 Oct 2026.

Specification

EUDAMED

Device Name
Mitsu FST™ /Aspiron™Polyglactin 910 FST- Absorbable Poly (Glycolide/L-Lactide) Surgical Suture U.S.P.
Model / Reference
ME/BRC/019
Primary DI / UDI-DI
18906070901607, 18904255207742, 18904255235462, 18904255210308, 18904255204314, 18904255233130, 18906070902789, 18906070907333, 18904255200460, 18904255204345, 18904255210315, 18904255210322, 18904255243658, 18906070906695, 18906070906497, 18904255204321, 18904255205120, 18904255204420, 18906070901638, 18906070901584, 18904255236063, 18906070902826, 18904255210827, 18904255207766, 18904255214382, 18904255200651, 18906070906718, 18906070902796, 18904255204352, 18904255208534, 18904255204376, 18904255229447, 18904255204338, 18904255230412, 18904255240138, 18904255229430, 18904255230405, 18904255201764, 18904255207759, 18904255210957, 18904255214351, 18906070902802, 18904255201375, 18904255210339, 18904255223186, 18904255214375, 18904255207308, 18904255249551, 18904255232744, 18906070906664
Basic UDI-DI
89042552MES_PGF03VQ
Direct Marketing DI
18904255243658
18904255236063
18904255229447
18904255240138
18904255229430
18904255230405
18906070902802
18904255223186
18904255249551
EMDN Code
H010101020201, H010101020202, H010101020203
Device Class
Class III
EU market of registration
Bulgaria

Manufacturer details

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

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Properties

  • Sterile
  • Implantable
  • Reprocessed NoEUDAMEDYesEUDAMED

Other properties (10)

  • Reusable: No
  • Contains Latex: 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