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STYPRO® Sheet

by curasan AG

Ref 9350 000 020Model STYPRO® Sheet

STYPRO® Sheet (9350 000 020) is a Class III device made by Curasan AG, registered in EUDAMED on 23 May 2026 (Basic UDI-DI B-+ECUR935000002020), active as of 24 Oct 2026.

Active European Union

CE MDD

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-+ECUR935000002020 Basic UDI-DI +ECUR935000002020UDI-DIDate23 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
STYPRO® Sheet, 9350 000 020
Primary DI / UDI-DI
+ECUR935000002020
Basic UDI-DI
B-+ECUR935000002020
EMDN code
M040503 Gelatine sponge haemostatic dressings
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000008316

Similar devices in this category

Other devices filed under HAEMOSTATIC DRESSINGS.

Other devices from Curasan AG

See all devices from Curasan AG →

Properties

  • Supplied sterile
  • Implantable
  • Reprocessed single-use device
  • Contains animal tissues or cells
Other properties (8, all answered No)