FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040109899 · Model: 2020314 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
Henry Schein
Primary DI
10304040109899
Version / Model
2020314
Catalog Number
2020314
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2019-11-01
Public Version
1
Public Version Date
2019-11-11
Public Version Status
New
Public Device Record Key
46ad3308-73cd-471b-aa82-6f4b1654f76e

Device Description

OBTURATOR - OBT6 - SIZE 50 Obt 6pk - CHC5

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKM GUTTA-PERCHA

GMDN Terms

Code Name
47751 Warm-bonded endodontic obturation system obturator

Identifiers

Type ID
Primary 10304040109899
Unit of Use 00304040109892