FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040089917 · Model: 9007987 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Henry Schein
Primary DI
10304040089917
Version / Model
9007987
Catalog Number
9007987
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2019-05-29
Public Version
2
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
0d8f3024-63fa-48f7-9ccd-3e5b13d78fdf

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
Primary 10304040089917
Unit of Use 00304040089910

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
To be stored in dry and fresh place, protected from sunlight