FDA UDI In Commercial Distribution 🇺🇸 United States

NUPRO®

DI: D0031303221 · Model: 130322 · Dentsply Professional
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
NUPRO®
Primary DI
D0031303221
Version / Model
130322
Company Name
Dentsply Professional
Labeler DUNS
144140845
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
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
41da6296-db0d-45a5-b141-cc73813aa174

Device Description

NUPRO® 5% Sodium Fluoride White Varnish, Patient Dose Kit - Mint. Contents: Integrated Brush, 50 Patient Doses of 0.4g.

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
Yes
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 D0031303222
Primary D0031303221
Unit of Use D0031303220

Customer Contacts

Device Sizes

Type Value Unit Text
Weight 0.4 Gram

Storage Conditions

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