FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: H65820203171 · Model: 2020317 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Henry Schein
Primary DI
H65820203171
Version / Model
2020317
Catalog Number
2020317
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2020-06-18
Public Version
1
Public Version Date
2020-06-26
Public Version Status
New
Public Device Record Key
b0a8df73-bd13-4760-aaaf-f70ad8d915ea

Device Description

OBTURATOR - OBT20 - SIZE 30 Obt 20pk CHC3

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
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
Unit of Use H65820203179
Primary H65820203171