FDA UDI In Commercial Distribution 🇺🇸 United States

Herculite XRV

DI: 10841396104838 · Model: 29850 · Kerr Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Herculite XRV
Primary DI
10841396104838
Version / Model
29850
Catalog Number
29850
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
8c43ff58-686b-4944-9bb2-340be81d3a70

Device Description

Unidose; Enamel D4; 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 10841396104838
Unit of Use 00841396104831

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