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Probe

EUDAMEDFDA UDI

Class A (EU MDR)

Ref AV-BP5006D

by Diamond Diagnostics Inc

Identity

Trade Name
Probe EUDAMED
Sample Probe FDA UDI
Generic Name
Ion-selective analyser IVD FDA UDI
Device Name
Sample Probe EUDAMED
Model / Reference
AV-BP5006D EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00811403010394 EUDAMEDFDA UDI
Basic UDI-DI
081140301AVBP5006D4L EUDAMED
EMDN Code
W05020180 SAMPLES TRANSPORT, CONTAINERS - ACCESSORIES EUDAMED
GMDN Term
Ion-selective analyser 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Probe 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 994e9e4a-3e58-46f8-9a3e-682984cfeff7 61 fields · synced Jun 8, 2026
  • FDA UDI e89ed1b0-3abc-49b2-86b8-9606b914ba59 32 fields · synced May 30, 2026