Skip to content

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

by Meril Endo Surgery Pvt. Ltd. 607 variants

Ref ME/BRC/018

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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 0013 Date30 Jun 2026IssuedStatusWithdrawn No longer placed on the EU market expires 8 Oct 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
Mitsu™/Aspiron™ Polyglactin 910 - Absorbable Poly (Glycolide/L-Lactide) Surgical Suture U.S.P.
Model / Reference
ME/BRC/018
Primary DI / UDI-DI
18906070903052
Basic UDI-DI
89042552MES_PGN02WW
EMDN Code
H010101020201, H010101020202, H010101020203
Device Class
Class III

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