FDA UDI In Commercial Distribution 🇺🇸 United States

nordicAktiva

DI: 07090042059022 · Model: 1.3 · Nordicneurolab AS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
nordicAktiva
Primary DI
07090042059022
Version / Model
1.3
Company Name
Nordicneurolab AS
Labeler DUNS
671280238
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-22
Public Version
5
Public Version Date
2020-06-02
Public Version Status
Update
Public Device Record Key
9f8f73dd-99d7-4a2d-a4fb-82b0a190ce3a

Device Description

NordicNeuroLab’s nordicAktiva is a stimulus presentation and workflow software which controls the presentation of stimuli during fMRI exams and has been designed specifically with the clinical user in mind. With an intuitive interface and detailed, easy-to-follow instructions, the user is guided step-by-step through the process of presenting stimuli during MR image acquisition. nordicAktiva runs on the stimulus presentation PC to which the NNL fMRI Hardware System is connected. Through the latter audiovisual stimuli are presented to, and feedback is collected from the patient.

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LNH System, Nuclear Magnetic Resonance Imaging

GMDN Terms

Code Name
40872 MRI system application software

Identifiers

Type ID
Primary 07090042059022

Customer Contacts

Phone
+4755707095

Premarket Submissions

Submission Number Supplement Number
K092253 000