Primary Device ID | 00850044487004 |
NIH Device Record Key | 34aba50d-c8c0-4adb-9ab3-74af1aeb2d35 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Retia Medical |
Version Model Number | FG-011 |
Catalog Number | FG-011 |
Company DUNS | 025675871 |
Company Name | RETIA MEDICAL, LLC |
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 | true |
Serial Number | false |
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 | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com | |
Phone | (914) 594-1986 |
HAgashe@mkmventuresllc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850044487004 [Primary] |
DXG | Computer, Diagnostic, Pre-Programmed, Single-Function |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-01 |
Device Publish Date | 2023-02-21 |
00860001506402 | The Argos Cardiac Output monitoring device is intended for use on patients above the age of 18. |
00860001506457 | Drager Interface Cable (14-pin MDR) |
00860001506440 | GE Interface Cable (7-pin Mini-DIN) |
00860001506433 | Transducer Interface Cable |
00860001506426 | GE Interface Cable (9-pin PDM) |
00860001506419 | Philips Interface Cable (3.5 mm Stereo Jack) |
00860001506464 | Spacelabs Interface Cable |
00860001506471 | Argos LAN Connectivity Kit |
00860001506495 | Argos Monitor Power Supply and AC Cord |
00860001506488 | Argos Serial Connectivity Kit |
00850044487004 | Mindray Interface Cable |
00850044487011 | Nihon Kohden Interface Cable |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RETIA MEDICAL 98810388 not registered Live/Pending |
Retia Medical Systems, Inc. 2024-10-19 |
RETIA MEDICAL 98810024 not registered Live/Pending |
Retia Medical Systems, Inc. 2024-10-19 |