Skip to content

Silkus

by TI Medical Private Limited 108 variants

Ref TI/C-BRO/01Model Braided coated Silk suture with needle,Braided coated Silk suture without needle

Active European Union

CE MDR

Valid until

22 Mar 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SZUTEST Konformitätsbewertungsstelle 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 Number89042482SIL010MD Basic UDI-DI Date18 Aug 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2608201 Active

    Quality management system EU MDR

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Braided coated Silk suture
Model / Reference
Braided coated Silk suture with needle, Braided coated Silk suture without needle, TI/C-BRO/01
Primary DI / UDI-DI
08904248216143, 08909296016936, 08904248217676, 08909296017940, 08909296021572, 08904248217034, 08904248236530, 08909296004803, 08909296016950, 08909296020308, 08904248270350, 08904248269934, 08904248217256, 08909296020674, 08909296010231, 08904248217485, 08904248218024, 08904248215832, 08909296021541, 08904248216693, 08904248215887, 08909296018978, 08904248299436, 08904248270190, 08904248217164, 08904248286054, 08904248217706, 08904248268098, 08904248216570, 08909296021473, 08909296021480, 08904248215924, 08909296018008, 08909296021558, 08909296009952, 08904248216464, 08909296019364, 08909296019807, 08904248216136, 08909296019203, 08904248215993, 08904248258365, 08904248216907, 08904248289055, 08909296020278, 08904248275140, 08904248231641, 08904248284005, 08909296013362, 08904248217881
Basic UDI-DI
89042482SIL010MD
EMDN Code
H010202020301, H010202020302
Device Class
Class IIb
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

  • Nylus

    Class IIb

  • Solus 910

    Class III

  • Solus Swift 910

    Class III

  • Solus

    Class III

  • Barb-E

    Class III

  • Silkus

    Class IIb

See all devices from TI Medical Private Limited →

Properties

  • Sterile
  • Implantable
  • Sutures

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