FDA UDI In Commercial Distribution 🇺🇸 United States

L100 Go System

DI: 00815962020337 · Model: LG1-5Y00 · BIONESS INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
L100 Go System
Primary DI
00815962020337
Version / Model
LG1-5Y00
Company Name
BIONESS INC.
Labeler DUNS
182287727
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-22
Public Version
1
Public Version Date
2020-04-30
Public Version Status
New
Public Device Record Key
510dd143-940b-49d5-a862-20d992f5939d

Device Description

L100 Go System, Right

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

GMDN Terms

Code Name
35725 Gait-enhancement electrical stimulation system, external

Identifiers

Type ID
Primary 00815962020337

Customer Contacts

Storage Conditions

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