Philips Wearable Biosensor 989803196861

GUDID 20884838064953

Philips Medical Systems

Kinesiology ambulatory recorder
Primary Device ID20884838064953
NIH Device Record Key40d756a3-cce0-415c-8310-24a19d33a39d
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhilips Wearable Biosensor
Version Model Number989803196861
Catalog Number989803196861
Company DUNS078628040
Company NamePhilips Medical Systems
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(999)999-9999
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Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
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Phone+1(999)999-9999
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS120884838064953 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DRGTRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-03-05
Device Publish Date2016-11-25

On-Brand Devices [Philips Wearable Biosensor]

20884838085231989803200061
20884838064960989803196871
20884838064953989803196861

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