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BioFire® Global Fever Panel

FDA UDI

Class II (US FDA UDI)

by BioFire Defense, LLC

Identity

Trade Name
BioFire® Global Fever Panel FDA UDI
Generic Name
Multiple-type tropical pathogen nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
Device Name
BioFire® Global Fever Panel - IVD reagent kit containing 6 tests FDA UDI
Model / Reference
DFA2-ASY-0004 FDA UDI
Description
BioFire® Global Fever Panel - IVD reagent kit containing 6 tests FDA UDI

Identifiers

Catalog Number
DFA2-ASY-0004 FDA UDI
Primary DI / UDI-DI
00851458005242 FDA UDI
510(k) Number
DEN200043 FDA UDI
K220870 FDA UDI
FDA Product Code
QMV FDA UDI
GMDN Term
Multiple-type tropical pathogen nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3966 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple-type tropical pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)

BioFire® Global Fever Panel by BioFire Defense, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-type tropical pathogen nucleic acid IVD, kit, nucleic acid technique (NAT).

Cleared under the same submission

K220870 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BioFire Defense, LLC

Sources (1)

  • FDA UDI 069b320a-284f-4058-b376-b167df5f56cc 36 fields · synced Jun 8, 2026