Philips GoSafe 2 7150MHB

GUDID 00884838081475

7150MHB (GoSafe)

Lifeline Systems Company

Home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system Vulnerable patient home alert system
Primary Device ID00884838081475
NIH Device Record Keybf8b4f9c-e533-4680-b2ba-75fac7197e04
Commercial Distribution Discontinuation2017-10-04
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePhilips GoSafe 2
Version Model Number300000103361
Catalog Number7150MHB
Company DUNS080030042
Company NameLifeline Systems Company
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100884838081475 [Primary]

FDA Product Code

ILQSystem, communication, powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-10-04

On-Brand Devices [Philips GoSafe 2]

008848380848277150MHB (GoSafe)
008848380814757150MHB (GoSafe)
008848380915737150MHB (GoSafe 2)
008848380936387250 (GoSafe 2)

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