Nipro Set Blood Tubing Set BL+A430/V912

GUDID 40383790008806

Blood Tubing Set for use with the SURDIAL DX Hemodialysis System

NIPRO MEDICAL CORPORATION

Haemodialysis blood tubing set, single-use
Primary Device ID40383790008806
NIH Device Record Key50145193-0bf3-48a5-b3c2-fb4ea782cdd9
Commercial Distribution StatusIn Commercial Distribution
Brand NameNipro Set Blood Tubing Set
Version Model NumberA430/V912
Catalog NumberBL+A430/V912
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 Usetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100383790008808 [Primary]
GS140383790008806 [Package]
Contains: 00383790008808
Package: case [24 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 Date2020-08-03
Device Publish Date2020-07-24

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