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Sample Probe

FDA UDI

by DIAMOND DIAGNOSTICS Inc

Identity

Trade Name
Sample Probe FDA UDI
Generic Name
Multiple clinical chemistry analyser IVD, laboratory FDA UDI
Model / Reference
RO-1043864D FDA UDI

Identifiers

Primary DI / UDI-DI
00811403018345 FDA UDI
GMDN Term
Multiple clinical chemistry analyser IVD, laboratory FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Multiple clinical chemistry analyser IVD, laboratory

Sample Probe by DIAMOND DIAGNOSTICS Inc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple clinical chemistry analyser IVD, laboratory.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ec432965-f928-44dd-9a68-9312fdf5698d 32 fields · synced May 30, 2026