FDA UDI In Commercial Distribution 🇺🇸 United States

StimRouter Electrode Set

DI: 00815962020047 · Model: ST2-7000 · BIONESS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
StimRouter Electrode Set
Primary DI
00815962020047
Version / Model
ST2-7000
Company Name
BIONESS INC.
Labeler DUNS
182287727
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-19
Public Version
5
Public Version Date
2021-09-20
Public Version Status
Update
Public Device Record Key
0a87ff9f-db12-40ba-b4c2-46d4f0e4cd7e

Device Description

Electrode Set

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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GZF STIMULATOR, PERIPHERAL NERVE, IMPLANTED (PAIN RELIEF)

GMDN Terms

Code Name
65318 Transcutaneous electrical stimulation electrode, reusable

Identifiers

Type ID
Primary 00815962020047

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
25 – 85 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Special Storage Condition, Specify
Special Conditions
Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
KiloPascal
Type
Storage Environment Temperature
Temperature Range
5 – 27 Degrees Celsius