Philips GoSafe 7000MHB

GUDID 00884838085909

7000MHB (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 ID00884838085909
NIH Device Record Keyc1fa3a9a-ea2a-4eb7-b0e2-1d2e5b38898e
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhilips GoSafe
Version Model Number300000367071
Catalog Number7000MHB
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
GS100884838085909 [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 Date2017-06-26

On-Brand Devices [Philips GoSafe]

008848380859097000MHB (GoSafe)
008848380848107100MHB (GoSafe)
008848380814687100MHB (GoSafe)
008848380915807100MHB (GoSafe)

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