| Primary Device ID | 03661540216206 |
| NIH Device Record Key | c3ea5826-a985-4671-beb9-84828535ed03 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PHOSPHORUS |
| Version Model Number | PHOS-0230 |
| Company DUNS | 267732378 |
| Company Name | ELITECH CLINICAL SYSTEMS SAS |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03661540216206 [Primary] |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2023-07-06 |
| Device Publish Date | 2016-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PHOSPHORUS 90623821 not registered Live/Pending |
Phosphorus Cybersecurity Inc. 2021-04-05 |
![]() PHOSPHORUS 87083408 5215288 Live/Registered |
PHOSPHORUS, INC. 2016-06-24 |
![]() PHOSPHORUS 85479035 not registered Dead/Abandoned |
White Oak Technologies, Inc. 2011-11-22 |