NXView Touch Monitor NX3302-A

GUDID M535NX3302A0

NXSTAGE MEDICAL, INC.

Haemodialysis system, institutional/home-use
Primary Device IDM535NX3302A0
NIH Device Record Key6a432245-d75f-4294-9caf-15ef20ed0939
Commercial Distribution StatusIn Commercial Distribution
Brand NameNXView Touch Monitor
Version Model NumberNX3302-A
Catalog NumberNX3302-A
Company DUNS088013219
Company NameNXSTAGE MEDICAL, INC.
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-866-697-8243
Emailinfo@nxstage.com

Operating and Storage Conditions

Storage Environment HumidityBetween 0 Percent (%) Relative Humidity and 93 Percent (%) Relative Humidity

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM535NX3302A0 [Primary]

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 Date2020-03-19
Device Publish Date2020-03-11

Devices Manufactured by NXSTAGE MEDICAL, INC.

10842289103044 - NxStage PureFlow Solution2024-04-04
10842289103051 - NxStage PureFlow Solution2024-04-04
10842289103068 - NxStage PureFlow Solution2024-04-04
10842289103075 - NxStage PureFlow Solution2024-04-04
10842289103082 - NxStage PureFlow Solution2024-04-04
10842289103099 - NxStage PureFlow Solution2024-04-04
10842289103105 - NxStage PureFlow Solution2024-04-04
10842289103112 - NxStage PureFlow Solution2024-04-04

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