← Back to catalogue

Aqaurius

FDA UDI

Class II (US FDA UDI)

by Ivoclar Vivadent, Inc.

Identity

Trade Name
Aqaurius FDA UDI
Generic Name
Dental brazing alloy FDA UDI
Device Name
Aquarius Ceramic Solder FDA UDI
Model / Reference
NA1192004 FDA UDI
Description
Aquarius Ceramic Solder FDA UDI

Identifiers

Catalog Number
NA1192004 FDA UDI
Primary DI / UDI-DI
D707NA11920040 FDA UDI
FDA Product Code
EJS FDA UDI
GMDN Term
Dental brazing 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 brazing alloy

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

Similar devices

Also classified as Dental brazing alloy.

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

Sources (1)

  • FDA UDI 6a878d6e-e5d5-4103-8ffc-d3a92cf2368e 34 fields · synced Jun 9, 2026