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 |