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TriageHF™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
TriageHF™ FDA UDI
Generic Name
Implantable cardiac device management application software FDA UDI
Device Name
SOFTWARE 5242 TRIAGEHF US FDA UDI
Model / Reference
5242 FDA UDI
Description
SOFTWARE 5242 TRIAGEHF US FDA UDI

Identifiers

Primary DI / UDI-DI
00763000351656 FDA UDI
PMA Number
P890003 FDA UDI
FDA Product Code
NVZ FDA UDI
GMDN Term
Implantable cardiac device management application software FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Implantable cardiac device management application software

TriageHF™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable cardiac device management application software.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI c361a016-4f82-4ee1-896f-2949ecfa19c0 35 fields · synced May 30, 2026