Nerveana+®

GUDID NVPTKITDCS5

NEUROVISION MEDICAL PRODUCTS, INC.

Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use
Primary Device IDNVPTKITDCS5
NIH Device Record Keybc21588c-5807-4d71-920c-b6d6738613a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameNerveana+®
Version Model NumberN/A
Company DUNS182057401
Company NameNEUROVISION MEDICAL PRODUCTS, INC.
Device Count5
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB006NVPTKITDCS1 [Unit of Use]
HIBCCB006NVPTKITDCS52 [Primary]
HIBCCNVPTKITDCS5 [Package]
Contains: B006NVPTKITDCS52
Package: [5 Units]
In Commercial Distribution

FDA Product Code

ETNStimulator, Nerve

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-28
Device Publish Date2023-04-20

On-Brand Devices [Nerveana+®]

NVPIC6NONE
NVPFKITMFT5NONE
NVPFKITMF5NONE
NVPFKITMDT5NONE
NVPFKITMD5NONE
NVPTKITDCST5N/A
NVPTKITDCS5N/A
NVPTKITDCLT5N/A
NVPTKITDCL5N/A
NVPTKITC3P8T5N/A
NVPTKITC3P85N/A
NVPTKITC3P7T5N/A
NVPTKITC3P75N/A
NVPTKITC3P6T5N/A
NVPTKITC3P65N/A
B006NVPTST2N/A
B600NVPS2NONE
B600NVPMS2NONE
B006NVPUSB1NONE
NVPTKITDCSWF5NONE
NVPTKITDCSD5N/A
NVPTKITDCLWF5NONE
NVPTKITDCLD5N/A
NVPTKITC3P8WSF5N/A
NVPTKITC3P7WSF5N/A
B006NVPTKITC3P6WSF5N/A
B006NVPT1NONE
B006NVPSTST2NONE
B006NVPMK1NONE

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