Synapsys VHIT 10739

GUDID 08054187380822

Video Head Impulse Test device

INVENTIS SRL

Dynamic visual acuity testing system
Primary Device ID08054187380822
NIH Device Record Keybf9491d3-9ca0-4e25-afea-da648ba461a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameSynapsys VHIT
Version Model NumberSynapsys VHIT Plus
Catalog Number10739
Company DUNS338454995
Company NameINVENTIS SRL
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it
Phone+39 0498962844
Emailquality@inventis.it

Device Identifiers

Device Issuing AgencyDevice ID
GS108054187380822 [Primary]

FDA Product Code

GWNNystagmograph

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-01-16
Device Publish Date2025-01-08

On-Brand Devices [Synapsys VHIT]

08054187380822Video Head Impulse Test device
08054187380815Video Head Impulse Test device

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