Primary Device ID | 07290013820389 |
NIH Device Record Key | fe46a470-760c-4b4a-aa2a-33e323e3f375 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Neurovirtual |
Version Model Number | 9002N-L90 |
Company DUNS | 600632715 |
Company Name | S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD |
Device Count | 2 |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290013819581 [Unit of Use] |
GS1 | 07290013820389 [Primary] |
MNR | Ventilatory Effort Recorder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-20 |
07290013820419 | 9102NS |
07290013820396 | 9010N |
07290013820389 | 9002N-L90 |
07290013820372 | 9002N-L120 |
07290013820334 | 9101NS |
07290013820327 | 9101N |
07290013820112 | 9102N |
07290013820044 | 1561N |
07290013819987 | 14830N |
07290013819888 | 1401NS |
07290013819871 | 1401N |
07290013819765 | 1250NS |
07290013819758 | 1250N |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEUROVIRTUAL 78922440 not registered Dead/Abandoned |
Neurovirtual USA, Inc. 2006-07-05 |
NEUROVIRTUAL 77204897 3378310 Live/Registered |
Neurovirtual USA, Inc. 2007-06-13 |