FDA UDI In Commercial Distribution 🇺🇸 United States

L300 Go System

DI: 00815962020207 · Model: L4T-5000 · BIONESS INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
L300 Go System
Primary DI
00815962020207
Version / Model
L4T-5000
Company Name
BIONESS INC.
Labeler DUNS
182287727
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-14
Public Version
5
Public Version Date
2020-09-17
Public Version Status
Update
Public Device Record Key
e109fe2f-33f6-4301-9da9-f2a8573a6240

Device Description

L300 Go System, Right Thigh Stand-Alone

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
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
35725 Gait-enhancement electrical stimulation system, external

Identifiers

Type ID
Primary 00815962020207

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190285 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – 55 Degrees Celsius