FDA UDI In Commercial Distribution 🇺🇸 United States

Bioness L300 Go Hydrogel Electrodes Set

DI: 00815962020078 · Model: LG3-5F00 · BIONESS INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bioness L300 Go Hydrogel Electrodes Set
Primary DI
00815962020078
Version / Model
LG3-5F00
Company Name
BIONESS INC.
Labeler DUNS
182287727
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-13
Public Version
4
Public Version Date
2021-03-31
Public Version Status
Update
Public Device Record Key
c835a12a-ba40-4aa6-b557-d8dee3e2c8ea

Device Description

Hydrogel Electrode Set

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
Yes
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
IPF Stimulator, muscle, powered
GZI STIMULATOR, NEUROMUSCULAR, EXTERNAL FUNCTIONAL

GMDN Terms

Code Name
65318 Transcutaneous electrical stimulation electrode, reusable

Identifiers

Type ID
Primary 00815962020078

Customer Contacts