← Back to catalogue

642E Centrifuge, Cardinal

FDA UDI

Class I (US FDA UDI)

by Drucker Diagnostics

Identity

Trade Name
642E Centrifuge, Cardinal FDA UDI
Generic Name
General-purpose centrifuge IVD FDA UDI
Device Name
General purpose laboratory centrifuge for sample separation. FDA UDI
Model / Reference
CA018104 FDA UDI
Description
General purpose laboratory centrifuge for sample separation. FDA UDI

Identifiers

Catalog Number
CA018104 FDA UDI
Primary DI / UDI-DI
00810052862194 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
General-purpose centrifuge IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose centrifuge IVD

642E Centrifuge, Cardinal by Drucker Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose centrifuge IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Drucker Diagnostics

Sources (1)

  • FDA UDI 54ec9b70-3614-498b-8f3b-b6c205b7b4ed 34 fields · synced Jun 1, 2026