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Tarmo Ensiapupakkaus

by Tammer Brands Oy 2 variants

Ref 210668, 315751

Active European Union

CE MDR

Valid until

Not listed

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

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 Number643005474210668AM Basic UDI-DI Date17 Oct 2022RegisteredStatusActive

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  • Withdrawn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

Model / Reference
210668, 315751
Primary DI / UDI-DI
06430054746687, 06430054747516
Basic UDI-DI
643005474210668AM, 643005474315751BR
EMDN Code
M9099 General and specialist medical devices – other (suture patches see h900102)
Device Class
Class I
Medical Purpose
Ensiapupakkaus

Manufacturer details

EUDAMED SRN
FI-PR-000029481

Other devices from Tammer Brands Oy

Properties

Other properties (1)

  • Sterile: No