Primary Device ID | 00085412095646 |
NIH Device Record Key | 0d8fc68f-5f11-444b-b0eb-b2a6f5dd0d57 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Duplocath |
Version Model Number | 921022 |
Catalog Number | 921022 |
Company DUNS | 005146311 |
Company Name | BAXTER INTERNATIONAL INC. |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
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 | |
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 |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Length | 25 Centimeter |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00085412095646 [Primary] |
FMF | Syringe, piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-10-12 |
20085412600042 | Catheter for the simultaneous application of Baxter's two-component fibrin sealant in endoscopic |
50085412600036 | Catheter for the simultaneous application of Baxter two-component fibrin sealant in minimally in |
20085412600028 | Catheter for the simultaneous application of Baxter's two-component fibrin sealant in areas of t |
00085412314112 | Duplocath Application Catheter |
00085412314105 | Duplocath Application Catheter with M.I.S. Adaptor |
00085412095646 | Duplocath Application Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DUPLOCATH 75327893 2312263 Live/Registered |
Baxter International Inc. 1997-07-21 |