FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10884389830338 · Model: MDSM611505 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
5

Basic Information

Brand Name
Medline
Primary DI
10884389830338
Version / Model
MDSM611505
Catalog Number
MDSM611505
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-12-10
Public Version
1
Public Version Date
2020-12-18
Public Version Status
New
Public Device Record Key
33ae4283-2f8f-429b-95ad-37023261674a

Device Description

ELECTRODE,FOAM,MONITORING,SLD GEL,5 PK

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
No
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 20884389830335
Primary 10884389830338
Package 40884389830339
Package 30884389830332
Unit of Use 50884389830336

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight, Protect from freezing, avoid excessive heat