Patient Safety Net

GUDID 00843997012065

MASIMO CORPORATION

Multiple-patient intensive/general healthcare physiologic monitoring system
Primary Device ID00843997012065
NIH Device Record Keya6ecfb52-3b34-4f17-a730-ec0473152b67
Commercial Distribution StatusIn Commercial Distribution
Brand NamePatient Safety Net
Version Model Number25375
Company DUNS780421038
Company NameMASIMO 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 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

Phone+1(949)297-7498
EmailTechService-US@masimo.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100843997012065 [Primary]

FDA Product Code

MSXSYSTEM,NETWORK AND COMMUNICATION,PHYSIOLOGICAL MONITORS

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-02-06
Device Publish Date2016-09-23

Devices Manufactured by MASIMO CORPORATION

00843997017688 - Nomoline2024-03-27 NomoLine LH Bypass Tubing, 3m
00843997005364 - Masimo W12024-03-11 Masimo W1, Tele-Health, Global
00843997017480 - Masimo W12024-03-11 Masimo W1, Global, France
00843997017497 - Masimo W12024-03-11 Masimo W1, Global, German
00843997017503 - Masimo W12024-03-11 Masimo W1, Global, Switzerland
00843997017510 - Masimo W12024-03-11 Masimo W1, Global, Italy
00843997017527 - Masimo W12024-03-11 Masimo W1, Global, Sweden
00843997017534 - Masimo W12024-03-11 Masimo W1, Global, Netherlands

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