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AutoMate 800 Sample Processor

FDA UDI

Class I (US FDA UDI)

by Beckman Coulter, Inc.

Identity

Trade Name
AutoMate 800 Sample Processor FDA UDI
Generic Name
Specimen processing instrument IVD FDA UDI
Device Name
AutoMate 800 Sample Processor FDA UDI
Model / Reference
AutoMate 800 Sample Processor FDA UDI
Description
AutoMate 800 Sample Processor FDA UDI

Identifiers

Catalog Number
A20743 FDA UDI
Primary DI / UDI-DI
15099590589813 FDA UDI
FDA Product Code
JQP FDA UDI
GMDN Term
Specimen processing instrument IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2100 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Specimen processing instrument IVD

AutoMate 800 Sample Processor by Beckman Coulter, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Specimen processing instrument IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e1cdfa3-ab86-470b-aae4-9323c7a8d3e0 36 fields · synced Jun 8, 2026