← Back to catalogue

Panther Fusion®

FDA UDI

Class II (US FDA UDI)

by Hologic, Inc.

Identity

Trade Name
Panther Fusion® FDA UDI
Generic Name
Multiple-genus respiratory virus nucleic acid IVD, control FDA UDI
Device Name
Panther Fusion® SARS-CoV-2/Flu A/B/RSV Assay Controls Kit. FDA UDI
Model / Reference
KIT, SARS/FLU A/B/RSV CONTROLS, FUSION, IVD FDA UDI
Description
Panther Fusion® SARS-CoV-2/Flu A/B/RSV Assay Controls Kit. FDA UDI

Identifiers

Catalog Number
PRD-07401 FDA UDI
Primary DI / UDI-DI
15420045515376 FDA UDI
510(k) Number
K222736 FDA UDI
FDA Product Code
QOF FDA UDI
GMDN Term
Multiple-genus respiratory virus nucleic acid IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3981 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple-genus respiratory virus nucleic acid IVD, control

Panther Fusion® by Hologic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-genus respiratory virus nucleic acid IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI 216d08a4-30dd-4385-9b71-866f3a006a37 37 fields · synced May 30, 2026