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Sangool - Patch 8 Sutura

by Eurosirel Spa

Part of a family of 8 devices: see the family page

Ref CSS122171Model CSS

Sangool - Patch 8 Sutura (CSS122171) is a Class I device made by Eurosirel Spa, registered in EUDAMED on 8 Jul 2026 (Basic UDI-DI 8017990CSSH3), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8017990CSSH3 Basic UDI-DI 08017990122171UDI-DIDate8 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Sterile plaster for suture
Model / reference
CSS, CSS122171
Primary DI / UDI-DI
08017990122171
Basic UDI-DI
8017990CSSH3
EMDN code
H900102 Bandages for sutures
Device class
Class I
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
IT-MF-000005982

Similar devices in this category

Other devices filed under BANDAGES FOR SUTURES.

Other devices from Eurosirel Spa

See all devices from Eurosirel Spa →

Properties

  • Supplied sterile
Other properties (13, all answered No)