FDA UDI In Commercial Distribution 🇺🇸 United States

Super Seal

DI: B1321002980 · Model: 100298 · PHOENIX DENTAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Super Seal
Primary DI
B1321002980
Version / Model
100298
Company Name
PHOENIX DENTAL, INC.
Labeler DUNS
004701368
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2022-06-27
Public Version Status
Update
Public Device Record Key
b9d5c55b-3a83-4bba-b19a-d83f5fd944e2

Device Description

Potassium oxalate based film forming acid resistant liner and desensitizer.

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
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
EJK Liner, Cavity, Calcium Hydroxide

GMDN Terms

Code Name
64794 Dental coating, tooth-desensitizing, professional

Identifiers

Type ID
Primary B1321002980

Customer Contacts

Phone
877-463-9905

Device Sizes

Type Value Unit Text
Total Volume 8 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature. Do not refrigerate.