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

by Meril Endo Surgery Pvt. Ltd. 607 variants

Ref ME/BRC/018

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 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  • Withdrawn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 20 May 2014

Last checked 23 Oct 2026.

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
18906070905674, 18906070903106, 18904255213590, 18904255213965, 18904255229546, 18904255205045, 18904255207582, 18904255249612, 18904255201429, 18906070901218, 18904255222936, 18904255230023, 18906070908361, 18904255210216, 18904255203553, 18906070903809, 18904255212128, 18904255206172, 18906070903816, 18906070906886, 18904255213712, 18904255207094, 18904255208060, 18904255213545, 18906070908187, 18906070901164, 18904255207544, 18906070906305, 18906070906411, 18906070905612, 18906070907043, 18906070905575, 18906070903076, 18904255223483, 18904255212609, 18904255224725, 18906070901423, 18904255213668, 18904255233246, 18904255207261, 18904255201351, 18906070907791, 18906070908866, 18904255208176, 18904255227894, 18904255210186, 18904255224602, 18904255207490, 18904255223001, 18904255225265
Basic UDI-DI
89042552MES_PGN02WW
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

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