FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 00304040063248 · Model: 1009592 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
Henry Schein
Primary DI
00304040063248
Version / Model
1009592
Catalog Number
1009592
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2019-11-04
Public Version
1
Public Version Date
2019-11-12
Public Version Status
New
Public Device Record Key
4f154a53-d39e-415b-8852-454da9ae853e

Device Description

Endoflex Reamers 25 mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EKP REAMER, PULP CANAL, ENDODONTIC

GMDN Terms

Code Name
31878 Manual endodontic file/rasp, reusable

Identifiers

Type ID
Primary 00304040063248
Unit of Use 10304040063245