PeritX 50-9510

GUDID 10885403222412

PeritX Drainage Kit - 2000 ml

CAREFUSION 2200, INC

Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle Closed-wound/centesis drainage receptacle
Primary Device ID10885403222412
NIH Device Record Key06e0da1a-0a9a-40a8-a0af-99a69a864f97
Commercial Distribution StatusIn Commercial Distribution
Brand NamePeritX
Version Model Number50-9510
Catalog Number50-9510
Company DUNS832696038
Company NameCAREFUSION 2200, INC
Device Count1
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com
Phone+1(800)323-9088
EmailCustomer_Support@BD.com

Device Dimensions

Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter
Total Volume2000 Milliliter

Device Identifiers

Device Issuing AgencyDevice ID
GS110885403222412 [Primary]
GS150885403222410 [Package]
Package: Case [5 Units]
In Commercial Distribution

FDA Product Code

PNGPeritoneal, drainage catheter for refractory ascites, long-term indwelling

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-11-13
Device Publish Date2017-06-12

On-Brand Devices [PeritX]

10885403222412PeritX Drainage Kit - 2000 ml
10885403222726PeritX Drainage Bag - 2000ml
50885403502048PeritX Peritoneal Catheter Kit, For Peritoneal Placement
10885403501838PeritX Peritoneal Catheter and Starter Kit, For Peritoneal Placement Only and For Patient Home U
50885403500846PeritX Valve Kit, For PeritX Peritoneal Catheter Only
50885403500839PeritX Peritoneal Catheter Mini Kit

Trademark Results [PeritX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PERITX
PERITX
88788681 not registered Live/Pending
CareFusion 2200, Inc.
2020-02-07
PERITX
PERITX
87086516 not registered Live/Pending
CareFusion 2200, Inc.
2016-06-28
PERITX
PERITX
85797231 not registered Dead/Abandoned
CareFusion 2200, Inc.
2012-12-07

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