Primary Device ID | 00085412002750 |
NIH Device Record Key | 0f7ac167-4f76-4b4f-a523-0d338008cf8b |
Commercial Distribution Discontinuation | 2023-09-19 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | DUO-VENT |
Version Model Number | 2C7552 |
Catalog Number | 2C7552 |
Company DUNS | 005083209 |
Company Name | BAXTER HEALTHCARE CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
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)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00085412002750 [Primary] |
GS1 | 50085412002755 [Package] Package: CASE [48 Units] Discontinued: 2018-09-19 Not in Commercial Distribution |
FPA | Set, administration, intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2025-10-06 |
Device Publish Date | 2016-09-24 |
00085412002750 - DUO-VENT | 2025-10-06Nitroglycerin Set with DUO-VENT Spike, PVC Tubing Segment, Injection Site, Male Luer Lock Adapter |
00085412002750 - DUO-VENT | 2025-10-06 Nitroglycerin Set with DUO-VENT Spike, PVC Tubing Segment, Injection Site, Male Luer Lock Adapter |
50197886011239 - Novum IQ | 2025-09-02 The Novum IQ Large Volume Pump (LVP) is a large volume infusion pump system that provides delivery of fluids into a patient in a |
50197886013172 - Novum IQ | 2025-09-02 The Novum IQ Large Volume Pump (LVP) is a large volume infusion pump system that provides delivery of fluids into a patient in a |
50197886013189 - Novum IQ | 2025-09-02 The Novum IQ Large Volume Pump (LVP) is a large volume infusion pump system that provides delivery of fluids into a patient in a |
50197886013196 - Novum IQ | 2025-09-02 The Novum IQ Large Volume Pump (LVP) is a large volume infusion pump system that provides delivery of fluids into a patient in a |
20197886002304 - Novum IQ | 2025-07-15 The Novum IQ Syringe Pump is software controlled Syringe infusion pump system that provides delivery of fluids into a patient in |
20197886008207 - Novum IQ | 2025-07-15 The Novum IQ Syringe Pump is software controlled Syringe infusion pump system that provides delivery of fluids into a patient in |
20197886008214 - Novum IQ | 2025-07-15 The Novum IQ Syringe Pump is software controlled Syringe infusion pump system that provides delivery of fluids into a patient in |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DUO-VENT 79025176 3280161 Dead/Cancelled |
Walker, Mark 2006-03-17 |
![]() DUO-VENT 79025176 3280161 Dead/Cancelled |
Sedelmeier, Joachim 2006-03-17 |
![]() DUO-VENT 78044438 2710134 Live/Registered |
BAXTER INTERNATIONAL INC. 2001-01-23 |
![]() DUO-VENT 77880674 not registered Dead/Abandoned |
Gilkey Window Company, Inc. 2009-11-25 |
![]() DUO-VENT 72140124 0757570 Dead/Expired |
HARTFORD GUN CHOKE COMPANY INCORPORATED 1962-03-19 |