FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040141202 · Model: 1019488 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
120

Basic Information

Brand Name
Henry Schein
Primary DI
10304040141202
Version / Model
1019488
Catalog Number
1019488
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
120
Record Status
Published
Publish Date
2021-01-28
Public Version
1
Public Version Date
2021-02-05
Public Version Status
New
Public Device Record Key
40a573c0-03dd-49d4-8006-d0b90bc71ca3

Device Description

Maxima Gutta Percha Points CC

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
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
EKM GUTTA-PERCHA

GMDN Terms

Code Name
45081 Synthetic gutta-percha

Identifiers

Type ID
Unit of Use 00304040141205
Primary 10304040141202