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Tris-tricin buffer (5 x konc.) pH 8, 6

by SSI Diagnostica A/S

Ref 44284

Active European Union

CE IVDR

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5713106CM_GeneralZL Basic UDI-DI 05713106442845UDI-DIDate14 May 2025RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device name
Culture Media - General agar plates and tubes
Model / reference
44284
Primary DI / UDI-DI
05713106442845
Basic UDI-DI
5713106CM_GeneralZL
EMDN code
W0104010805 Buffers
Device class
Class A
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
DK-MF-000023933

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Properties

  • Contains animal tissues or cells
  • Contains substances of microbial origin
  • Reagent
  • Professional testing

Other properties (9)

  • Supplied sterile: No
  • Sterilise before use: No
  • Contains human tissues or cells: No
  • IVD kit: No
  • Self-testing: No
  • Near-patient testing: No
  • Companion diagnostics: No
  • IVD instrument: No
  • New device: No