FDA UDI Not in Commercial Distribution 🇺🇸 United States

VivoTab Electrode (3 pack)

DI: 00627908070050 · Model: 100001 · Vivosonic Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VivoTab Electrode (3 pack)
Primary DI
00627908070050
Version / Model
100001
Company Name
Vivosonic Inc
Labeler DUNS
201740425
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-05
Public Version
3
Public Version Date
2020-04-21
Public Version Status
Update
Public Device Record Key
78efa17e-ee53-44a3-88a3-640a850caa6d
Distribution End Date
2020-04-20

Device Description

Electrodes for use with the Integrity and Aurix system (DI: 00627908020017 and 00627908080011respectively). The UDI is comprised of the following: GTIN (01) + EXPIRY (17) + BATCH/LOT (10)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
GWJ Stimulator, Auditory, Evoked Response

GMDN Terms

Code Name
35747 Evoked-potential audiometer

Identifiers

Type ID
Primary 00627908070050