Relivion

GUDID 17290018393014

Electrode Pad Set

NEUROLIEF LTD

Electrical probe/electrode conductive pad
Primary Device ID17290018393014
NIH Device Record Key53ad4f65-9128-431b-b4cc-712f7ceecc4e
Commercial Distribution StatusIn Commercial Distribution
Brand NameRelivion
Version Model NumberPAD0001A
Company DUNS600484465
Company NameNEUROLIEF LTD
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107290018393017 [Primary]
GS117290018393014 [Package]
Contains: 07290018393017
Package: Cardboard box [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PCCStimulator, Nerve, Electrical, Transcutaneous, For Migraine

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-12-13
Device Publish Date2021-12-05

On-Brand Devices [Relivion]

17290018393014Electrode Pad Set
17290018393113Relivion is a non-invasive medical device. It transfers mild electrical pulses to branches of th

Trademark Results [Relivion]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RELIVION
RELIVION
88005409 5823083 Live/Registered
Neurolief Ltd.
2018-06-19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.