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Electrode

EUDAMEDFDA UDI

Class A (EU MDR)

Ref OY-MU9194D

by Diamond Diagnostics Inc

Identity

Trade Name
Electrode EUDAMED
Sodium Electrode FDA UDI
Generic Name
Sodium (Na+) electrode IVD FDA UDI
Device Name
Na+ Electrode AU EUDAMED
Model / Reference
OY-MU9194D EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00811403017058 EUDAMEDFDA UDI
Basic UDI-DI
081140301OYMU9194DT5 EUDAMED
EMDN Code
W0580 IVD GENERAL USE CONSUMABLES DEVICES - OTHER ACCESSORIES EUDAMED
GMDN Term
Sodium (Na+) electrode IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Market of Registration
Hungary EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Electrode by DIAMOND DIAGNOSTICS Inc — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000035435
Authorised Representative
Diamond Diagnostics Inc. Magyarországi Fióktelepe HU-AR-000034351

Sources (2)

  • EUDAMED 52f7886b-09a8-4bea-98ee-ff4f1f4af2f4 61 fields · synced Jul 24, 2026
  • FDA UDI c2b6dc8c-2673-40aa-b48d-c3b26624ae7a 32 fields · synced May 30, 2026