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Ammonia

EUDAMED

Class IVD General (EU MDR)

Ref Amo-Mk-0620

by Ns Biotec

Identity

Trade Name
Ammonia EUDAMED
Device Name
Ammonia EUDAMED
Model / Reference
Amo-Mk-0620 EUDAMED

Identifiers

Primary DI / UDI-DI
D-Ammonia8B EUDAMED
Basic UDI-DI
B-Ammonia8B EUDAMED
EMDN Code
W01010301 AMMONIA EUDAMED

Classification

Device Class
Class IVD General EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Ammonia by Ns Biotec — 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

Manufacturer
Ns Biotec
EUDAMED SRN
EG-MF-000032515
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED cce5b616-f4f0-46e8-ba90-24780e274b75 61 fields · synced Jun 18, 2026