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Sample cup

EUDAMEDFDA UDI

Class A (EU MDR)

Ref BM-409041D

by Diamond Diagnostics Inc

Identity

Trade Name
Sample cup EUDAMED
Sample Cups FDA UDI
Generic Name
Assay container IVD, single-use FDA UDI
Device Name
Sample Cups, 3mL EUDAMED
Model / Reference
BM-409041D EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00811403011872 EUDAMEDFDA UDI
Basic UDI-DI
081140301BM409041DDW EUDAMED
EMDN Code
W05020180 SAMPLES TRANSPORT, CONTAINERS - ACCESSORIES EUDAMED
GMDN Term
Assay container IVD, single-use 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Sample cup 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 fac16a28-0c3c-42d5-b89c-ac586cee9869 61 fields · synced Jun 18, 2026
  • FDA UDI b206b645-84be-4fca-aaa4-05520c7e426c 32 fields · synced May 30, 2026