FDA UDI In Commercial Distribution 🇺🇸 United States

Red Dot™

DI: 10707387569607 · Model: 2259-50 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Red Dot™
Primary DI
10707387569607
Version / Model
2259-50
Catalog Number
2259-50
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
5af3a690-3db1-429f-96ef-95d3d5119d76

Device Description

3M™ Red Dot™ Foam Monitoring Electrode, 50/Bag, 20/Case, 36/Plt 2259-50

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
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
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 50707387569605
Primary 10707387569607
Unit of Use 00707387232535

Customer Contacts