FDA UDI In Commercial Distribution 🇺🇸 United States

Herculite Ultra

DI: 10841396104142 · Model: 35160 · Kerr Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Herculite Ultra
Primary DI
10841396104142
Version / Model
35160
Catalog Number
35160
Company Name
Kerr Corporation
Labeler DUNS
199354556
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-08-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
c2e9133a-535c-4440-99d9-7f7bf2f9ba1e

Device Description

Nanohybrid Composite Restorative; Unidose; Enamel B4; Refill

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
EBF MATERIAL, TOOTH SHADE, RESIN

GMDN Terms

Code Name
38764 Light-cured dental restorative composite resin

Identifiers

Type ID
Primary 10841396104142
Unit of Use 00841396104145

Customer Contacts

Phone
+18005377123

Device Sizes

Type Value Unit Text
Weight 4 Gram

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at ambient temperature