FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040099466 · Model: 5701167 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Henry Schein
Primary DI
10304040099466
Version / Model
5701167
Catalog Number
5701167
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2018-12-18
Public Version
1
Public Version Date
2019-01-18
Public Version Status
New
Public Device Record Key
dec7bf69-a601-4d2d-80a0-6aa1b0b6909c

Device Description

General Monitoring Radiolucent Foam Electrode with Carbon Snap

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
Yes
MRI Safety
MR Conditional
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
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Primary 10304040099466
Unit of Use 00304040099469