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Sample diluent

EUDAMEDFDA UDI

Class A (EU MDR)

Ref DA-S635D

by Diamond Diagnostics Inc

Identity

Trade Name
Sample diluent EUDAMED
Quick IMT Sample Diluent FDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
Sample Diluent IMT EUDAMED
Model / Reference
DA-S635D EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00811403014217 EUDAMEDFDA UDI
Basic UDI-DI
081140301DAS635DKE EUDAMED
EMDN Code
W05020180 SAMPLES TRANSPORT, CONTAINERS - ACCESSORIES EUDAMED
GMDN Term
Buffered sample diluent 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

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

Sample diluent 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 5941643a-c6c2-4984-a922-0cf14b558bd1 61 fields · synced Jun 19, 2026
  • FDA UDI 917517e8-f518-440b-8de4-d01d93df3dd8 32 fields · synced May 30, 2026