FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277657694 · Model: MDS611930AG · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277657694
Version / Model
MDS611930AG
Catalog Number
MDS611930AG
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-08
Public Version
1
Public Version Date
2020-12-16
Public Version Status
New
Public Device Record Key
bfcbca04-774c-4e51-a7f3-9e693f3a25d6

Device Description

ELECTRODE,ECG,FOAM,STRESS,30/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
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 40888277657695
Package 20888277657691
Package 30888277657698
Primary 10888277657694

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K020003 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Away from Sunlight. Protect from Freezing; Avoid Excessive Heat