FDA UDI In Commercial Distribution 🇺🇸 United States

NUPRO®

DI: D0031302121 · Model: 130212 · Dentsply Professional
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
500

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Basic Information

Brand Name
NUPRO®
Primary DI
D0031302121
Version / Model
130212
Company Name
Dentsply Professional
Labeler DUNS
144140845
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
27524798-493d-484c-8928-192fd92ec246

Device Description

NUPRO® 5% Sodium Fluoride White Varnish, Grape. Contents: 500 Patient Doses of 0.4g, 500 Brush Applicators, and 3 Prophy Grips.

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
No
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
LBH VARNISH, CAVITY

GMDN Terms

Code Name
35698 Dental cavity varnish

Identifiers

Type ID
Package D0031302122
Primary D0031302121
Unit of Use D0031302120

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry. Keep out of sunlight.
Type
Storage Environment Temperature
Temperature Range
5 – 25 Degrees Celsius