FDA UDI Not in Commercial Distribution 🇺🇸 United States

AdvanTrode

DI: 00677346310232 · Model: WT152 · PEPIN MANUFACTURING, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
4

Basic Information

Brand Name
AdvanTrode
Primary DI
00677346310232
Version / Model
WT152
Company Name
PEPIN MANUFACTURING, INC.
Labeler DUNS
807703996
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2016-10-05
Public Version
5
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
f59f5a9f-7f3f-42ec-aae8-99044b1b6739
Distribution End Date
2019-02-05

Device Description

1.5" x 2" (4cm x 5cm) Rectangle

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
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 00677346320231
Primary 00677346310232
Unit of Use 00677346300233

Premarket Submissions

Submission Number Supplement Number
K070807 000