| Primary Device ID | 20884450372948 |
| NIH Device Record Key | bc533302-b54c-420e-820e-732908ea0451 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Safedraw™ |
| Version Model Number | 10884450372941 |
| Catalog Number | 688076/B |
| Company DUNS | 595138793 |
| Company Name | ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450372944 [Unit of Use] |
| GS1 | 10884450372941 [Primary] |
| GS1 | 20884450372948 [Package] Contains: 10884450372941 Package: [5 Units] In Commercial Distribution |
| DXN | System, measurement, blood-pressure, non-invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-09-26 |
| Device Publish Date | 2019-09-18 |
| 20884450388710 | 10884450388713 |
| 20884450372535 | 10884450372538 |
| 20884450372948 | 10884450372941 |
| 20884450372511 | 10884450372514 |
| 20884450481114 | 10884450481117 |
| 20884450360594 | 10884450360597 |
| 20884450544154 | 10884450544157 |
| 20884450372788 | 10884450372781 |
| 20884450409019 | 10884450409012 |
| 20884450385108 | 10884450385101 |
| 20884450384804 | 10884450384807 |
| 20884450372801 | 10884450372804 |
| 20884450360600 | 10884450360603 |
| 20884450327665 | 10884450327668 |
| 20884450327054 | 10884450327057 |
| 20884450326613 | 10884450326616 |
| 20884450326606 | 10884450326609 |
| 20884450326590 | 10884450326593 |
| 20884450326583 | 10884450326586 |
| 20884450326446 | 10884450326449 |
| 20884450326439 | 10884450326432 |
| 20884450326422 | 10884450326425 |
| 20884450326415 | 10884450326418 |
| 20884450621152 | 10884450621155 |
| 20884450619296 | 10884450619299 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SAFEDRAW 78349783 2920800 Live/Registered |
MERIT MEDICAL SYSTEMS, INC. 2004-01-09 |