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Harmony Medium

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent, Inc.

Identity

Trade Name
Harmony Medium FDA UDI
Generic Name
Dental casting noble alloy FDA UDI
Device Name
Harmony Medium 1oz/31g FDA UDI
Model / Reference
582003 FDA UDI
Description
Harmony Medium 1oz/31g FDA UDI

Identifiers

Catalog Number
582003 FDA UDI
Primary DI / UDI-DI
D7075820030 FDA UDI
FDA Product Code
EJT FDA UDI
GMDN Term
Dental casting noble alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3060 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: Dental casting noble alloy

Harmony Medium by Ivoclar Vivadent, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental casting noble alloy.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0dea21a5-4324-49d1-ad8a-6410f2468a00 34 fields · synced Jun 9, 2026