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MicroScan

FDA UDI

Class I (US FDA UDI)

by Beckman Coulter, Inc.

Identity

Trade Name
MicroScan FDA UDI
Generic Name
Photometer, absorbance/transmission, automated FDA UDI
Device Name
MicroScan autoSCAN-4 Instrument (Reconditioned) FDA UDI
Model / Reference
B1012-2A-E FDA UDI
Description
MicroScan autoSCAN-4 Instrument (Reconditioned) FDA UDI

Identifiers

Primary DI / UDI-DI
15099590655433 FDA UDI
FDA Product Code
JJQ FDA UDI
GMDN Term
Photometer, absorbance/transmission, automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2300 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Photometer, absorbance/transmission, automated

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

Similar devices

Also classified as Photometer, absorbance/transmission, automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 45b5f93f-817b-4cf9-aed8-e05e06d06e8a 33 fields · synced Jun 8, 2026