FDA UDI Not in Commercial Distribution 🇺🇸 United States

NESS L300-Plus System

DI: 07290110483012 · Model: L3P-5000 · BIONESS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NESS L300-Plus System
Primary DI
07290110483012
Version / Model
L3P-5000
Catalog Number
501-00123-01
Company Name
BIONESS INC.
Labeler DUNS
182287727
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-02
Public Version
5
Public Version Date
2021-09-20
Public Version Status
Update
Public Device Record Key
c609d6f7-fc75-4568-ada9-8e1b00871bf9
Distribution End Date
2017-09-30

Device Description

L300 Plus US System Kit, Right (regular)

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

GMDN Terms

Code Name
35725 Gait-enhancement electrical stimulation system, external

Identifiers

Type ID
Primary 07290110483012

Customer Contacts

Phone
+97297907100 ext. 100

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-25 – 55 Degrees Celsius