Careflow™ 681631/A

GUDID 20884450321502

ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.

Peripheral artery cannula
Primary Device ID20884450321502
NIH Device Record Key87fcc87a-f99e-4b79-9f01-2967403a9550
Commercial Distribution StatusIn Commercial Distribution
Brand NameCareflow™
Version Model Number10884450321505
Catalog Number681631/A
Company DUNS595138793
Company NameARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.
Device Count10
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100884450321508 [Unit of Use]
GS110884450321505 [Primary]
GS120884450321502 [Package]
Contains: 10884450321505
Package: [10 Units]
In Commercial Distribution

FDA Product Code

FOZCatheter, intravascular, therapeutic, short-term less than 30 days

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-28
Device Publish Date2022-09-20

On-Brand Devices [Careflow™]

2088445032179310884450321796
2088445032180910884450321802
2088445035788410884450357887
2088445032909610884450329099
2088445032192210884450321925
2088445032190810884450321901
2088445032187810884450321871
2088445032181610884450321819
2088445032189210884450321895
2088445037924410884450379247
2088445032176210884450321765
2088445032159510884450321598
2088445032156410884450321567
2088445032188510884450321888
2088445032150210884450321505

Trademark Results [Careflow]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CAREFLOW
CAREFLOW
98050445 not registered Live/Pending
Careflow LLC
2023-06-20
CAREFLOW
CAREFLOW
97826864 not registered Live/Pending
ViiNetwork, Inc.
2023-03-07
CAREFLOW
CAREFLOW
97594230 not registered Live/Pending
Bamboo Health, Inc.
2022-09-16
CAREFLOW
CAREFLOW
88324504 not registered Dead/Abandoned
AccentCare, Inc.
2019-03-04
CAREFLOW
CAREFLOW
87356998 5415736 Live/Registered
Vital Solutions GmbH
2017-03-03
CAREFLOW
CAREFLOW
87015820 not registered Live/Pending
Midmark Corporation
2016-04-27
CAREFLOW
CAREFLOW
86206765 not registered Dead/Abandoned
Covidien LP
2014-02-27
CAREFLOW
CAREFLOW
77669399 3733541 Dead/Cancelled
HIT Consulting Services
2009-02-12
CAREFLOW
CAREFLOW
77669362 3833437 Live/Registered
MAGNUS HEALTH, LLC
2009-02-12
CAREFLOW
CAREFLOW
75530195 not registered Dead/Abandoned
CareFlow / Net, Inc.
1998-07-31

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.