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Solus 910

by TI Medical Private Limited 410 variants

Ref TI/C-BRO/01Model Braided Coated Polyglactin 910 Suture with needle (Violet)

Active European Union

CE MDR

Valid until

22 Mar 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier SZUTEST Konformitätsbewertungsstelle GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2975-MED-2608201 Date23 Mar 2026IssuedStatusActive expires 22 Mar 2031

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 2975-MED-2608201 Active

    Quality management system EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    23 Mar 2026
    Expires
    22 Mar 2031
  • 2975-MED-2608201-D01 Active

    Technical documentation EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    23 Mar 2026
    Expires
    22 Mar 2031

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 32 countries, as listed in EUDAMED:

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

  • Austria since 9 Jun 2016
  • Belgium since 9 Jun 2016
  • Bulgaria since 9 Jun 2016
  • Croatia since 9 Jun 2016
  • Cyprus since 9 Jun 2016
  • Czechia since 9 Jun 2016
  • Denmark since 9 Jun 2016
  • Estonia since 9 Jun 2016
  • Finland since 9 Jun 2016
  • France since 9 Jun 2016
  • Germany since 9 Jun 2016
  • Greece since 9 Jun 2016
  • Hungary since 9 Jun 2016
  • Iceland since 9 Jun 2016
  • Ireland since 9 Jun 2016
  • Italy since 9 Jun 2016
  • Latvia since 9 Jun 2016
  • Liechtenstein since 9 Jun 2016
  • Lithuania since 9 Jun 2016
  • Luxembourg since 9 Jun 2016
  • Malta since 9 Jun 2016
  • Netherlands since 9 Jun 2016
  • Northern Ireland since 9 Jun 2016
  • Norway since 9 Jun 2016
  • Poland since 9 Jun 2016
  • Portugal since 9 Jun 2016
  • Romania since 9 Jun 2016
  • Slovakia since 9 Jun 2016
  • Slovenia since 9 Jun 2016
  • Spain since 9 Jun 2016
  • Sweden since 9 Jun 2016
  • Türkiye since 9 Jun 2016

Last checked 27 Oct 2026.

Specification

EUDAMED

Device Name
Braided Coated Polyglactin 910 Suture
Model / Reference
Braided Coated Polyglactin 910 Suture with needle (Violet), TI/C-BRO/01
Primary DI / UDI-DI
08904248203815
Basic UDI-DI
89042482SOL003PJ
EMDN Code
H010101020201 Polyglycolic with lactic acid multifilament with needle for open surgery
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IN-MF-000026561
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from TI Medical Private Limited

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See all devices from TI Medical Private Limited →

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