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Reference solution

EUDAMEDFDA UDI

Class A (EU MDR)

Ref SM-B01417351D

by Diamond Diagnostics Inc

Identity

Trade Name
Reference solution EUDAMED
ISE Reference Solution FDA UDI
Generic Name
Multiple electrolyte IVD, reagent FDA UDI
Device Name
ISE Reference Solution ADVIA EUDAMED
Model / Reference
SM-B01417351D EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00811403018949 EUDAMEDFDA UDI
Basic UDI-DI
081140301SMB01417351DZB EUDAMED
EMDN Code
W0101050399 CALIBRATORS AND STANDARDS (CLINICAL CHEMISTRY) - OTHER EUDAMED
GMDN Term
Multiple electrolyte IVD, reagent 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Reference solution 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 2b69a0e5-7091-499b-b79e-b394f5dfe297 61 fields · synced Jun 19, 2026
  • FDA UDI 68abb2ce-6af0-4c6a-912c-8ffc8cc11905 32 fields · synced May 30, 2026