FDA UDI In Commercial Distribution 🇺🇸 United States

Auragen™

DI: 10381780036364 · Model: AU4X5P12 · INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Auragen™
Primary DI
10381780036364
Version / Model
AU4X5P12
Company Name
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
Labeler DUNS
531408342
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
6ef80a15-1ced-4419-b2a5-8f99685dfa1c

Device Description

The AURAGEN™ Cortical Surface Electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are placed on the exposed cortical surface or inserted into the subdural space to contact the cortical surface. Cortical Electrodes are available with platinum contacts and vary in size according to the number of contacts. The type of cortical electrode used is dependent on the procedure and the size of area being tested.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GYC ELECTRODE, CORTICAL

GMDN Terms

Code Name
32545 Cortical electrode

Identifiers

Type ID
Secondary M272AU4X5P121
Primary 10381780036364

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082250 000
K926424 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 20 platinum contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room temperature