Careflow™ 681714/A
GUDID 20884450321878
ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.
Central venous catheterization kit, short-term| Primary Device ID | 20884450321878 |
| NIH Device Record Key | 82e95ccf-cc3f-4c7e-8344-e1830c561531 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Careflow™ |
| Version Model Number | 10884450321871 |
| Catalog Number | 681714/A |
| Company DUNS | 595138793 |
| Company Name | ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. |
| Device Count | 5 |
| 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 | 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450321874 [Unit of Use] |
| GS1 | 10884450321871 [Primary] |
| GS1 | 20884450321878 [Package] Contains: 10884450321871 Package: [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K033500
FDA Product Code
| FOZ | Catheter,intravascular,therapeutic,short-term less than 30 days |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2021-02-05 |
| Device Publish Date | 2018-03-01 |
On-Brand Devices [Careflow™]
| 20884450321793 | 10884450321796 |
| 20884450321809 | 10884450321802 |
| 20884450357884 | 10884450357887 |
| 20884450329096 | 10884450329099 |
| 20884450321922 | 10884450321925 |
| 20884450321908 | 10884450321901 |
| 20884450321878 | 10884450321871 |
| 20884450321816 | 10884450321819 |
| 20884450321892 | 10884450321895 |
| 20884450379244 | 10884450379247 |
| 20884450321762 | 10884450321765 |
| 20884450321595 | 10884450321598 |
| 20884450321564 | 10884450321567 |
| 20884450321885 | 10884450321888 |
| 20884450321502 | 10884450321505 |
Trademark Results [Careflow]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CAREFLOW 98050445 not registered Live/Pending |
Careflow LLC 2023-06-20 |
 CAREFLOW 97826864 not registered Live/Pending |
ViiNetwork, Inc. 2023-03-07 |
 CAREFLOW 97594230 not registered Live/Pending |
Bamboo Health, Inc. 2022-09-16 |
 CAREFLOW 88324504 not registered Dead/Abandoned |
AccentCare, Inc. 2019-03-04 |
 CAREFLOW 87356998 5415736 Live/Registered |
Vital Solutions GmbH 2017-03-03 |
 CAREFLOW 87015820 not registered Live/Pending |
Midmark Corporation 2016-04-27 |
 CAREFLOW 86206765 not registered Dead/Abandoned |
Covidien LP 2014-02-27 |
 CAREFLOW 77669399 3733541 Dead/Cancelled |
HIT Consulting Services 2009-02-12 |
 CAREFLOW 77669362 3833437 Live/Registered |
MAGNUS HEALTH, LLC 2009-02-12 |
 CAREFLOW 75530195 not registered Dead/Abandoned |
CareFlow / Net, Inc. 1998-07-31 |
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