FDA UDI In Commercial Distribution 🇺🇸 United States

L300 Go System

DI: 00810188050342 · Model: LG3-5F00 · Bioness Medical, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
L300 Go System
Primary DI
00810188050342
Version / Model
LG3-5F00
Company Name
Bioness Medical, Inc.
Labeler DUNS
119378513
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-17
Public Version
1
Public Version Date
2025-07-25
Public Version Status
New
Public Device Record Key
32e22c11-bd20-49cc-83be-d484cbf622a1

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
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
IPF Stimulator, Muscle, Powered
GZI Stimulator, Neuromuscular, External Functional

GMDN Terms

Code Name
65318 Transcutaneous electrical stimulation electrode, reusable

Identifiers

Type ID
Primary 00810188050342
Previous 00815962020078

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190285 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 27 Degrees Celsius