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BioCode 2500 Multiplex Detection System

FDA UDI

Class I (US FDA UDI)

by Applied BioCode, Inc.

Identity

Trade Name
BioCode 2500 Multiplex Detection System FDA UDI
Generic Name
Microplate reader IVD, semi-automated FDA UDI
Device Name
The BioCode 2500 Multiplex Detection System is a digital optics imaging system for use with Applied BioCode’s Barcoded Magnetic Beads (BMB) technology. FDA UDI
Model / Reference
1 FDA UDI
Description
The BioCode 2500 Multiplex Detection System is a digital optics imaging system for use with Applied BioCode’s Barcoded Magnetic Beads (BMB) technology. FDA UDI

Identifiers

Catalog Number
41-A0005 FDA UDI
Primary DI / UDI-DI
00851034007059 FDA UDI
FDA Product Code
JJQ FDA UDI
GMDN Term
Microplate reader IVD, semi-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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Microplate reader IVD, semi-automated

BioCode 2500 Multiplex Detection System by Applied BioCode, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microplate reader IVD, semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Applied BioCode, Inc.

Sources (1)

  • FDA UDI de484c86-b8b1-4451-959b-fd332a5ef95d 36 fields · synced May 30, 2026