FDA UDI In Commercial Distribution 🇺🇸 United States

Instrumentation Difra

DI: B516221280 · Model: NysStar I · Instrumentation Difra SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Instrumentation Difra
Primary DI
B516221280
Version / Model
NysStar I
Catalog Number
22128
Company Name
Instrumentation Difra SA
Labeler DUNS
370173410
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-19
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
644d48c2-b2a0-4d12-a743-29e35c947a9e

Device Description

The videonystagmography performed by a camera and infra red light measures and records the eye movement, which is analyzed by the software. NYSSTAR I is the essential tool to study the various functions of balance, namely the oculomotricity (ocular saccades, pursuit, optokinetic nystagmus) and the study of the vestibular system (spontaneous and positional nystagmi, rotary tests, caloric tests). NYSSTAR I is able to record all eye movements, as well horizontal, as vertical and even rotary movements on option. The calibration carried out by NYSSTAR I is stable and should only be made once at the beginning of the examination. The recording by camera removes all artefacts due to the changes of polarity between the electrodes and the skin like with the interferences of electric and electrophysiological origin.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
GWN Nystagmograph

GMDN Terms

Code Name
11479 Electronystagmograph

Identifiers

Type ID
Primary B516221280

Premarket Submissions

Submission Number Supplement Number
K070670 000