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Ammonia

EUDAMED

Class IVD General (EU MDR)

Ref D-645 002Ref D-645 003

by Kalians Corporation

Identity

Trade Name
Ammonia EUDAMED
Device Name
Ammonia EUDAMED
Model / Reference
D-645 002 EUDAMED
D-645 003 EUDAMED

Identifiers

Primary DI / UDI-DI
62230182710934 EUDAMED
62230182711092 EUDAMED
Basic UDI-DI
B-62230182710934 EUDAMED
B-62230182711092 EUDAMED
EMDN Code
W01010301 AMMONIA EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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 Kalians Corporation — 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
Kalians Corporation
EUDAMED SRN
EG-MF-000050142
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 41d873b6-dd65-49f8-9839-257cb523f433 61 fields · synced Jul 13, 2026
  • EUDAMED d6e20d13-8379-4052-bab1-c717e769dba2 61 fields · synced May 19, 2026