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Valve

EUDAMEDFDA UDI

Class A (EU MDR)

Ref ME-2108D

by Diamond Diagnostics Inc

Identity

Trade Name
Valve EUDAMED
Solution Valve FDA UDI
Generic Name
Reference electrode IVD FDA UDI
Device Name
Solutions Valve EUDAMED
Model / Reference
ME-2108D EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00811403015849 EUDAMEDFDA UDI
Basic UDI-DI
081140301ME2108DDJ EUDAMED
FDA Product Code
JGS FDA UDI
CEM FDA UDI
EMDN Code
W05020180 SAMPLES TRANSPORT, CONTAINERS - ACCESSORIES EUDAMED
GMDN Term
Reference electrode IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class II FDA UDI
Regulation Number
862.1665 FDA UDI
862.1600 FDA UDI
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

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Valve 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 9c0d79ba-d5a7-47b0-91f0-66b7258065d0 61 fields · synced Jun 19, 2026
  • FDA UDI 58065748-6d56-4483-a776-2ac2978c8bca 32 fields · synced May 30, 2026