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Deben Salmonella Antisera

EUDAMED

Class IVD General (EU MDR)

Ref 290779Model H-z15

by Deben Diagnostics Ltd

Identity

Device Name
Deben Salmonella Antisera EUDAMED
Model / Reference
H-z15 EUDAMED
290779 EUDAMED

Identifiers

Primary DI / UDI-DI
05061053152035 EUDAMED
Basic UDI-DI
B-05061053152035 EUDAMED
EMDN Code
W01029001 ANTISERA (MONOVALENT AND POLYVALENT) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Malta EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Deben Salmonella Antisera by Deben Diagnostics Ltd — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
GB-MF-000023695
Authorised Representative
EU-UK Authorised Representative Ltd XI-AR-000010192

Sources (1)

  • EUDAMED 1b975f89-dd7e-44c0-b615-7fe6286583fe 61 fields · synced Jun 19, 2026