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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
Exogenous DNA/RNA internal control IVD, kit FDA UDI
Device Name
Panther Fusion® Internal Control-X. FDA UDI
Model / Reference
INTERNAL CONTROL-X, 960T, IVD FDA UDI
Description
Panther Fusion® Internal Control-X. FDA UDI

Identifiers

Catalog Number
PRD-04476 FDA UDI
Primary DI / UDI-DI
15420045510470 FDA UDI
FDA Product Code
NJR FDA UDI
GMDN Term
Exogenous DNA/RNA internal control IVD, kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3740 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: Exogenous DNA/RNA internal control IVD, kit

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

Similar devices

Also classified as Exogenous DNA/RNA internal control IVD, kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI 6eca6d64-7d7b-4900-9752-0f5f7242bf83 36 fields · synced Jun 7, 2026