FDA UDI In Commercial Distribution 🇺🇸 United States

Hexa

DI: 10850023750690 · Model: CU-2001 · Hexa Dental
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

Basic Information

Brand Name
Hexa
Primary DI
10850023750690
Version / Model
CU-2001
Catalog Number
CU-2001
Company Name
Hexa Dental
Labeler DUNS
096955608
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2023-03-28
Public Version
3
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
28daf3f1-281d-47b4-9aae-8aa0cc0dc64f

Device Description

Hexa Composite Enamel A1 Caplets (20)

Device Characteristics

Single Use
Yes
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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
62477 Dental composite resin kit

Identifiers

Type ID
Primary 10850023750690
Unit of Use 00850023750693
Package 20850023750697

Customer Contacts