Primary Device ID | 50885403502048 |
NIH Device Record Key | 57e5844d-e382-457b-bf3b-b9ab70ab2a16 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PeritX |
Version Model Number | 50-9000C |
Catalog Number | 50-9000C |
Company DUNS | 832696038 |
Company Name | CAREFUSION 2200, INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com | |
Phone | +1(800)323-9088 |
Customer_Support@BD.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10885403502040 [Primary] |
GS1 | 50885403502048 [Package] Contains: 10885403502040 Package: Case [10 Units] In Commercial Distribution |
PNG | Peritoneal, drainage catheter for refractory ascites, long-term indwelling |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-17 |
Device Publish Date | 2021-03-09 |
10885403222412 | PeritX Drainage Kit - 2000 ml |
10885403222726 | PeritX Drainage Bag - 2000ml |
50885403502048 | PeritX Peritoneal Catheter Kit, For Peritoneal Placement |
10885403501838 | PeritX Peritoneal Catheter and Starter Kit, For Peritoneal Placement Only and For Patient Home U |
50885403500846 | PeritX Valve Kit, For PeritX Peritoneal Catheter Only |
50885403500839 | PeritX Peritoneal Catheter Mini Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PERITX 88788681 not registered Live/Pending |
CareFusion 2200, Inc. 2020-02-07 |
PERITX 87086516 not registered Live/Pending |
CareFusion 2200, Inc. 2016-06-28 |
PERITX 85797231 not registered Dead/Abandoned |
CareFusion 2200, Inc. 2012-12-07 |