FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: H65810138641 · Model: 1013864 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
120

Basic Information

Brand Name
Henry Schein
Primary DI
H65810138641
Version / Model
1013864
Catalog Number
1013864
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
120
Record Status
Published
Publish Date
2022-10-15
Public Version
1
Public Version Date
2022-10-24
Public Version Status
New
Public Device Record Key
0e0869d4-2776-493f-a0e5-3097b01af69a

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
Yes
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 H65810138649
Primary H65810138641