FDA UDI Not in Commercial Distribution 🇺🇸 United States

CavityShield™

DI: 30605861038110 · Model: 12141 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
CavityShield™
Primary DI
30605861038110
Version / Model
12141
Catalog Number
12141
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2023-01-16
Public Version Status
Update
Public Device Record Key
37eecc4d-19eb-4703-be12-aebf5ba53599
Distribution End Date
2021-03-01

Device Description

3M™ ESPE™ CavityShield™ 5% Sodium Fluoride Varnish Mixed Dentition Clinic Pack - Bubble Gum Flavor, 12141

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 50605861038114
Primary 30605861038110
Unit of Use 00605861038119

Customer Contacts