FDA UDI In Commercial Distribution 🇺🇸 United States

OptraSculpt Pad Refill

DI: DVIV639792AN1 · Model: 639792AN · IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
60

Basic Information

Brand Name
OptraSculpt Pad Refill
Primary DI
DVIV639792AN1
Version / Model
639792AN
Catalog Number
639792AN
Company Name
IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Labeler DUNS
448015938
Distribution Status
In Commercial Distribution
Device Count in Pkg
60
Record Status
Published
Publish Date
2020-08-26
Public Version
4
Public Version Date
2023-09-01
Public Version Status
Update
Public Device Record Key
e3d73502-fa34-41b4-be5b-c09c5dfb55bb

Device Description

OptraSculpt Pad Refill

Device Characteristics

Single Use
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXR APPLICATOR, RESIN

GMDN Terms

Code Name
41861 Dental restoration carver, resin

Identifiers

Type ID
Unit of Use DIVO639792AN0
Primary DVIV639792AN1
Package DVIV639792AN2