| Primary Device ID | 00860001506495 |
| NIH Device Record Key | a1e694f5-a82b-4a33-ae28-db7667a77b8e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Retia Medical |
| Version Model Number | FG-010 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860001506495 [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 | 2022-01-06 |
| Device Publish Date | 2021-12-29 |
| 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 |