Pyxis

GUDID 10885403421532

Pyxis Transfusion Verification

CAREFUSION 303, INC.

Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software Blood bank information system application software
Primary Device ID10885403421532
NIH Device Record Keyb19ed5ec-b5f6-4e41-bc8f-bdc4aaa2eed6
Commercial Distribution Discontinuation2017-06-01
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePyxis
Version Model NumberTRANSFUSION
Company DUNS360624720
Company NameCAREFUSION 303, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com
Phone+1(888)812-3266
EmailProductComplaints@bd.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110885403421532 [Primary]

FDA Product Code

MMHSOFTWARE, BLOOD BANK, STAND ALONE PRODUCTS

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-04-20
Device Publish Date2016-12-08

On-Brand Devices [Pyxis]

10885403421532Pyxis Transfusion Verification
10885403512629MedStation 4000 MAIN

Trademark Results [Pyxis]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PYXIS
PYXIS
98106616 not registered Live/Pending
Kimberly-Clark Worldwide, Inc.
2023-07-28
PYXIS
PYXIS
97884053 not registered Live/Pending
IAM Robotics, LLC
2023-04-12
PYXIS
PYXIS
97793646 not registered Live/Pending
Nexgen Ventures, Inc
2023-02-14
PYXIS
PYXIS
97290120 not registered Live/Pending
GS Medical Co., Ltd.
2022-03-01
PYXIS
PYXIS
97079593 not registered Live/Pending
Pyxis, L.L.C.
2021-10-18
PYXIS
PYXIS
90501806 not registered Live/Pending
General Genomics Inc.
2021-02-01
PYXIS
PYXIS
88785440 not registered Live/Pending
BERKADIA PROPRIETARY HOLDING LLC
2020-02-05
PYXIS
PYXIS
88673797 not registered Live/Pending
Pyxis LLC
2019-10-30
PYXIS
PYXIS
88281657 not registered Live/Pending
ASSET PERFORMANCE NETWORKS, LLC
2019-01-29
PYXIS
PYXIS
87935202 5648276 Live/Registered
Pyxis, LLC
2018-05-24
PYXIS
PYXIS
87859913 5615978 Live/Registered
Pyxis Lab, INC
2018-04-02
PYXIS
PYXIS
87441896 not registered Live/Pending
Chauvet & Sons, LLC
2017-05-09

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