FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 20193489036371 · Model: MDSE3RDFP · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
4

Basic Information

Brand Name
Medline
Primary DI
20193489036371
Version / Model
MDSE3RDFP
Catalog Number
MDSE3RDFP
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2022-12-01
Public Version
1
Public Version Date
2022-12-09
Public Version Status
New
Public Device Record Key
86cba06b-8013-4cdc-9371-12ef2391cfce

Device Description

ELECTRODES,TENS,PLATINUM,FOAM, 3" RND

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
GXY Electrode, cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Package 30193489036378
Primary 20193489036371
Unit of Use 00193489036377

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 27 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry, Protect from freezing, Avoid excessive heat.
Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place.