VPX Vasopulse

GUDID 00860000214018

RESONANT SPECIFIC TECHNOLOGIES, INC.

Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered Physical therapy transcutaneous electrical stimulation system, line-powered
Primary Device ID00860000214018
NIH Device Record Keya9a7c7df-724a-4f1f-aaf1-f004cb38c552
Commercial Distribution StatusIn Commercial Distribution
Brand NameVPX Vasopulse
Version Model NumberVPX Vasopulse
Company DUNS109562944
Company NameRESONANT SPECIFIC TECHNOLOGIES, INC.
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com
Phone866-726-3927
Emailinfo@rstsanexas.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860000214018 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GZJStimulator, Nerve, Transcutaneous, For Pain Relief

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-05-23
Device Publish Date2019-04-25

Devices Manufactured by RESONANT SPECIFIC TECHNOLOGIES, INC.

00860000214056 - SynRG Light Pad2021-09-28
00860000214032 - RST-SANEXAS Basic2021-04-26
00860000214049 - RST-SANEXAS PT2021-04-26
00860000214025 - SynRG Light Pad2019-09-24
00860000214001 - neoGEN2019-05-23
00860000214018 - VPX Vasopulse2019-05-23
00860000214018 - VPX Vasopulse2019-05-23
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