FDA UDI Not in Commercial Distribution 🇺🇸 United States

Superdent® Eugenol U.S.P.

DI: D6871410504FG2 · Model: 1410504FG · DENTSPLY INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
Superdent® Eugenol U.S.P.
Primary DI
D6871410504FG2
Version / Model
1410504FG
Catalog Number
1410504FG
Company Name
DENTSPLY INTERNATIONAL INC.
Labeler DUNS
083235549
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2022-09-30
Public Version Status
Update
Public Device Record Key
2e9e3258-efcf-408e-ace1-bea157c1cf61
Distribution End Date
2019-01-09

Device Description

Superdent® Eugenol U.S.P. 4 oz.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
EMB ZINC OXIDE EUGENOL

GMDN Terms

Code Name
17610 Denture reliner, soft, professional

Identifiers

Type ID
Primary D6871410504FG2
Unit of Use D6871410504FG0

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 118 Milliliter
Device Size Text, specify 12 Bottles (4 oz/118mL)