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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
The DNA IC Probe ASR contains an oligonucleotide designed to detect the DNA target present in the Panther Fusion® Internal Control-S and Panther Fusion® Internal Control-X reagents. FDA UDI
Model / Reference
DNA, IC Probe (ASR) FDA UDI
Description
The DNA IC Probe ASR contains an oligonucleotide designed to detect the DNA target present in the Panther Fusion® Internal Control-S and Panther Fusion® Internal Control-X reagents. FDA UDI

Identifiers

Catalog Number
PRD-04308 FDA UDI
Primary DI / UDI-DI
15420045511408 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Exogenous DNA/RNA internal control IVD, kit 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

No

FDA UDI

Manufacturing Date

Yes

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 1e8c48d2-4dff-4e26-a702-6c9d696c5eaa 36 fields · synced Jun 6, 2026