FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: H65890079851 · Model: 9007985 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Henry Schein
Primary DI
H65890079851
Version / Model
9007985
Catalog Number
9007985
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2020-06-19
Public Version
2
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
e165e8fe-f647-4386-abe0-71ee285553aa

Device Description

Sectional Matrices 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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKF INSTRUMENT, CONTOURING, MATRIX, OPERATIVE

GMDN Terms

Code Name
16370 Dental wedge, reusable

Identifiers

Type ID
Unit of Use H65890079859
Primary H65890079851