FDA UDI Not in Commercial Distribution 🇺🇸 United States

Aquarius XH

DI: D7075766150 · Model: 576615 · IVOCLAR VIVADENT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Aquarius XH
Primary DI
D7075766150
Version / Model
576615
Catalog Number
576615
Company Name
IVOCLAR VIVADENT, INC.
Labeler DUNS
176935203
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-29
Public Version
3
Public Version Date
2024-11-29
Public Version Status
Update
Public Device Record Key
2cd590f5-c723-4f25-af36-0a19dc30442d
Distribution End Date
2024-11-28

Device Description

Aquarius XH 25 g

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EJT Alloy, gold-based noble metal

GMDN Terms

Code Name
35858 Dental casting noble alloy

Identifiers

Type ID
Primary D7075766150