FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 00304040107959 · Model: 5701355 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Henry Schein
Primary DI
00304040107959
Version / Model
5701355
Catalog Number
5701355
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2019-04-26
Public Version
1
Public Version Date
2019-05-06
Public Version Status
New
Public Device Record Key
f2aed98e-8cbd-4349-9de7-423cd8a6e96d

Device Description

Titanium post refill kit, Red, size 1. 10 titanium posts, 1 primary reamer, 1 secondary drill.

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
ELR POST, ROOT CANAL

GMDN Terms

Code Name
38609 Root canal post, preformed

Identifiers

Type ID
Primary 00304040107959
Unit of Use 10304040107956