FDA UDI In Commercial Distribution 🇺🇸 United States

Neon 12 KIT

DI: 05391530950091 · Model: TF01K · INCEREB LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Neon 12 KIT
Primary DI
05391530950091
Version / Model
TF01K
Company Name
INCEREB LIMITED
Labeler DUNS
985065024
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-24
Public Version
1
Public Version Date
2022-04-01
Public Version Status
New
Public Device Record Key
1a83af4d-07a2-428e-9c0b-069c048396c2

Device Description

Kit version of neon12, packaged without electrode paste or skin prep gel

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
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY Electrode, Cutaneous

GMDN Terms

Code Name
11440 Analytical scalp electrode, single-use

Identifiers

Type ID
Primary 05391530950091
Package 05391530950114
Package 05391530950138

Premarket Submissions

Submission Number Supplement Number
K151576 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 25 Degrees Celsius