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Panther Fusion®

FDA UDI

Class I (US FDA UDI)

by Hologic, Inc.

Identity

Trade Name
Panther Fusion® FDA UDI
Generic Name
Varicella-zoster virus (VZV) nucleic acid IVD, control FDA UDI
Device Name
Hologic VZV Plasmid Control. FDA UDI
Model / Reference
LBLD, VZV PLASMID (UNASSAYED CONTROL) FDA UDI
Description
Hologic VZV Plasmid Control. FDA UDI

Identifiers

Catalog Number
PRD-04996 FDA UDI
Primary DI / UDI-DI
15420045512146 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Varicella-zoster virus (VZV) nucleic acid IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Varicella-zoster virus (VZV) nucleic acid IVD, control

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

Similar devices

Also classified as Varicella-zoster virus (VZV) nucleic acid IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI afc2e32e-7aa7-40ed-a8dd-2029ffa60c3a 36 fields · synced May 31, 2026