Primary Device ID | 08054187380822 |
NIH Device Record Key | bf9491d3-9ca0-4e25-afea-da648ba461a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Synapsys VHIT |
Version Model Number | Synapsys VHIT Plus |
Catalog Number | 10739 |
Company DUNS | 338454995 |
Company Name | INVENTIS SRL |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it | |
Phone | +39 0498962844 |
quality@inventis.it |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08054187380822 [Primary] |
GWN | Nystagmograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-01-16 |
Device Publish Date | 2025-01-08 |
08054187380822 | Video Head Impulse Test device |
08054187380815 | Video Head Impulse Test device |