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MicroScan

FDA UDI

Class I (US FDA UDI)

by Beckman Coulter, Inc.

Identity

Trade Name
MicroScan FDA UDI
Generic Name
Microorganism identification/antimicrobial-susceptibility analyser IVD FDA UDI
Device Name
LabPro Data Management System FDA UDI
Model / Reference
V4.42 FDA UDI
Description
LabPro Data Management System FDA UDI

Identifiers

Primary DI / UDI-DI
15099590676872 FDA UDI
FDA Product Code
OUG FDA UDI
LON FDA UDI
GMDN Term
Microorganism identification/antimicrobial-susceptibility analyser IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 FDA UDI
866.1645 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microorganism identification/antimicrobial-susceptibility analyser IVD

MicroScan by Beckman Coulter, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microorganism identification/antimicrobial-susceptibility analyser IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beckman Coulter, Inc.

Sources (1)

  • FDA UDI fbe3c855-9810-453a-9b35-f23c0196884c 33 fields · synced Jun 8, 2026