FDA UDI In Commercial Distribution 🇺🇸 United States

Herculite Ultra

DI: 00841396103704 · Model: 34333 · Kerr Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Herculite Ultra
Primary DI
00841396103704
Version / Model
34333
Catalog Number
34333
Company Name
Kerr Corporation
Labeler DUNS
199354556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
5f0c105c-9299-4a0c-a3f6-f5f82d1b9a4b

Device Description

Nanohybrid Composite Restorative; Intro Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
35870 Dental composite resin

Identifiers

Type ID
Primary 00841396103704

Customer Contacts

Phone
+18005377123

Device Sizes

Type Value Unit Text
Weight 8.6 Gram

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
stored at ambient temperature OptiBond All-In-One refrigerated 2C to 8C (36-46F).