FDA UDI In Commercial Distribution 🇺🇸 United States

TENSPRODUCTS/TENSTRODE

DI: 00816924020044 · Model: KWF125o · Tensproducts, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
TENSPRODUCTS/TENSTRODE
Primary DI
00816924020044
Version / Model
KWF125o
Catalog Number
KWF125o-TP
Company Name
Tensproducts, LLC
Labeler DUNS
104307787
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-12
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
11ae7c5b-fc2f-4700-b5e0-8d4b63bb51de

Device Description

1.5" x 2.5" OVAL WHITE FOAM ELECTRODE 4/PK

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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 20816924020048
Primary 00816924020044
Package 10816924020041

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083302 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 95 Percent (%) Relative Humidity