Primary Device ID | 10801741075466 |
NIH Device Record Key | 13921263-cca2-4917-9c89-9551bb9a8fec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Securis |
Version Model Number | SECNS01 |
Catalog Number | SECNS01 |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, Inc. |
Device Count | 1000 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)545-0890 |
medical.services@crbard.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741075469 [Unit of Use] |
GS1 | 10801741075466 [Primary] |
KMK | DEVICE, INTRAVASCULAR CATHETER SECUREMENT |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-25 |
Device Publish Date | 2019-10-17 |
10801741075466 | SECURIS STABILIZATION DEVICE w/DFU, 1000 units, SECNS01 |
20801741075456 | SECURIS STABILIZATION DEVICE |
10801741085731 | DOT SECURIS STABN DEVICE SEPP W/ALCOHOL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SECURIS 88646794 not registered Live/Pending |
Velotec Sports LLC 2019-10-08 |
SECURIS 86322346 5082629 Live/Registered |
DRD TACTICAL LLC 2014-06-27 |
SECURIS 85905910 4645902 Live/Registered |
C. R. Bard, Inc. 2013-04-16 |
SECURIS 85536729 4378457 Live/Registered |
PC Recycler, Inc. 2012-02-08 |
SECURIS 85442042 4195954 Live/Registered |
CUSTOM SPINE ACQUISITION, INC. 2011-10-07 |
SECURIS 75272934 2208171 Live/Registered |
Securis Corporation 1997-04-11 |