Nipro Ultrafilter

GUDID 40383790008868

Filter for clean dialysate and water

NIPRO MEDICAL CORPORATION

Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter Haemodialysis system dialysate pyrogen filter
Primary Device ID40383790008868
NIH Device Record Keyde56023a-4683-49a4-82b4-6be52889bbdc
Commercial Distribution StatusIn Commercial Distribution
Brand NameNipro Ultrafilter
Version Model NumberCF+609N
Company DUNS797372554
Company NameNIPRO MEDICAL CORPORATION
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com
Phone908-393-7030
Emailinfo@nipromed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100383790008860 [Primary]
GS140383790008868 [Package]
Contains: 00383790008860
Package: case [12 Units]
In Commercial Distribution

FDA Product Code

KDIDialyzer, High Permeability With Or Without Sealed Dialysate System

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-27
Device Publish Date2020-07-17

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10383790000397 - Nipro SafeTouch TULIP Safety Fistula Needle2023-09-25 SafeTouch Tulip Safety AVF (15Gx1-1/4") 12" tube, rotating hub
00383790000406 - Nipro SafeTouch TULIP Safety Fistula Needle2023-09-25 SafeTouch Tulip Safety AVF (15Gx1") 12" tube, fixed hub (twin pack)
10383790000427 - Nipro SafeTouch TULIP Safety Fistula Needle2023-09-25 SafeTouch Tulip Safety AVF (16Gx1") 12" tube, fixed hub

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