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Dermapore

by Seyi̇tler Ki̇mya Sanayi̇ A.Ş. 11 variants

Part of a family of 93 devices: see the family page

Ref S305

Dermapore (S305) is a Class I device made by Seyi̇tler Ki̇mya Sanayi̇ A.Ş., registered in EUDAMED on 6 May 2026 (Basic UDI-DI 8699664FLSTHH), active as of 25 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8699664FLSTHH Basic UDI-DI 08699664030519UDI-DIDate6 May 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Surgical Tape
Model / reference
S305
Primary DI / UDI-DI
08699664030519
Basic UDI-DI
8699664FLSTHH
EMDN code
M050199 Surgical plasters - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019722

Similar devices in this category

Other devices filed under SURGICAL PLASTERS.

Other devices from Seyi̇tler Ki̇mya Sanayi̇ A.Ş.

See all devices from Seyi̇tler Ki̇mya Sanayi̇ A.Ş. →

Properties

Other properties (14, all answered No)