← Back to catalogue

Harmony™

FDA UDI

Class Unclassified (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Harmony™ FDA UDI
Generic Name
Pulmonary transcatheter heart valve bioprosthesis FDA UDI
Device Name
TPV HARMONY-22 COMM FDA UDI
Model / Reference
HARMONY-22 FDA UDI
Description
TPV HARMONY-22 COMM FDA UDI

Identifiers

Primary DI / UDI-DI
00763000338985 FDA UDI
PMA Number
P200046 FDA UDI
FDA Product Code
NPV FDA UDI
GMDN Term
Pulmonary transcatheter heart valve bioprosthesis FDA UDI

Classification

Device Class
Unclassified FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Pulmonary transcatheter heart valve bioprosthesis

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

Similar devices

Also classified as Pulmonary transcatheter heart valve bioprosthesis.

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
Medtronic, Inc.

Sources (1)

  • FDA UDI fcae176a-4ea0-45c2-b68d-1847e602f13d 37 fields · synced May 30, 2026