Acid connector cpl 10L jug

GUDID 00084086113014

Acid connector cpl 10L jug

Fresenius Medical Care Renal Therapies Group, LLC

Haemodialysis system, institutional
Primary Device ID00084086113014
NIH Device Record Keyc975d513-7245-48e5-a044-a13282c03994
Commercial Distribution StatusIn Commercial Distribution
Brand NameAcid connector cpl 10L jug
Version Model NumberF50044950
Company DUNS079732391
Company NameFresenius Medical Care Renal Therapies Group, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx
Phone1 (800) 227-2572
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100084086113014 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KDIDialyzer, High Permeability With Or Without Sealed Dialysate System

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-08-11
Device Publish Date2025-08-01

Devices Manufactured by Fresenius Medical Care Renal Therapies Group, LLC

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10840861102560 - 5008X2025-08-11 5008X HD Pre-Flush – Twister Blood Tubing Set
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