FDA UDI In Commercial Distribution 🇺🇸 United States

Bio Protech

DI: 00817120020517 · Model: 3838FCTZ(NST) · BIO PROTECH USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Bio Protech
Primary DI
00817120020517
Version / Model
3838FCTZ(NST)
Company Name
BIO PROTECH USA, INC.
Labeler DUNS
789127011
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-08
Public Version
3
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
b5f5666b-75fa-41b3-97b6-66b555d49bc1

Device Description

3838FCTZ(NST) - 38x38mm Electrodes, Foam, Carbon, Plastic Zip Lock

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 30817120020518
Package 20817120020511
Package 10817120020514
Primary 00817120020517

Customer Contacts

Phone
714-730-9950