Philips GoSafe 2 7150MHB

GUDID 00884838091573

7150MHB (GoSafe 2)

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 ID00884838091573
NIH Device Record Key8838582f-4fa9-4f2f-a6ae-dc79c49e5def
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhilips GoSafe 2
Version Model Number300002566981
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
GS100884838091573 [Primary]

FDA Product Code

ILQSystem, communication, powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-06-10
Device Publish Date2019-06-01

On-Brand Devices [Philips GoSafe 2]

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

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