Primary Device ID | 10885403512629 |
NIH Device Record Key | 7d8e3d99-5a06-43b5-a158-960ed7f0a9ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pyxis |
Version Model Number | 303 |
Company DUNS | 360624720 |
Company Name | CAREFUSION 303, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com | |
Phone | +1(800)727-6102 |
productcomplaints@bd.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10885403512629 [Primary] |
BRY | CABINET, TABLE AND TRAY, ANESTHESIA |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-30 |
Device Publish Date | 2022-11-22 |
10885403421532 | Pyxis Transfusion Verification |
10885403512629 | MedStation 4000 MAIN |
10885403477836 | Pyxis Anesthesia System ES |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PYXIS 98651174 not registered Live/Pending |
Vokamancy, Inc. 2024-07-16 |
![]() PYXIS 98106616 not registered Live/Pending |
Kimberly-Clark Worldwide, Inc. 2023-07-28 |
![]() PYXIS 97884053 not registered Live/Pending |
IAM Robotics, LLC 2023-04-12 |
![]() PYXIS 97793646 not registered Live/Pending |
Nexgen Ventures, Inc 2023-02-14 |
![]() PYXIS 97290120 not registered Live/Pending |
GS Medical Co., Ltd. 2022-03-01 |
![]() PYXIS 97079593 not registered Live/Pending |
Pyxis, L.L.C. 2021-10-18 |
![]() PYXIS 90501806 not registered Live/Pending |
General Genomics Inc. 2021-02-01 |
![]() PYXIS 88785440 not registered Live/Pending |
BERKADIA PROPRIETARY HOLDING LLC 2020-02-05 |
![]() PYXIS 88673797 not registered Live/Pending |
Pyxis LLC 2019-10-30 |
![]() PYXIS 88281657 not registered Live/Pending |
ASSET PERFORMANCE NETWORKS, LLC 2019-01-29 |
![]() PYXIS 87935202 5648276 Live/Registered |
Pyxis, LLC 2018-05-24 |
![]() PYXIS 87859913 5615978 Live/Registered |
Pyxis Lab, INC 2018-04-02 |