FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10884389943519 · Model: MDSM618350 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Medline
Primary DI
10884389943519
Version / Model
MDSM618350
Catalog Number
MDSM618350
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-10-14
Public Version
3
Public Version Date
2018-10-22
Public Version Status
Update
Public Device Record Key
b858f6d3-ecd3-411a-a71d-6a1c9e70a2c4

Device Description

ELECTRODE, FOAM, WET GEL, 50/PK, 6000/CS

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
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
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
11425 Electrode conductive medium

Identifiers

Type ID
Primary 10884389943519
Unit of Use 80884389943518

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Transient spike of 104F|Keep Away from sunlight|Protect from Freezing|Avoid Excessive Heat