Primary Device ID | NVPTKITDCSWF5 |
NIH Device Record Key | 0d7ddec6-afc3-4424-83fd-6021dfd5d242 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nerveäna+® |
Version Model Number | NONE |
Company DUNS | 182057401 |
Company Name | NEUROVISION MEDICAL PRODUCTS, INC. |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B006NVPTKITDCSWF5 [Unit of Use] |
HIBCC | B006NVPTKITDCSWF52 [Primary] |
HIBCC | NVPTKITDCSWF5 [Package] Contains: B006NVPTKITDCSWF52 Package: [5 Units] In Commercial Distribution |
IKT | Electrode, Needle, Diagnostic Electromyograph |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-09 |
Device Publish Date | 2024-02-01 |
NVPIC6 | NONE |
NVPFKITMFT5 | NONE |
NVPFKITMF5 | NONE |
NVPFKITMDT5 | NONE |
NVPFKITMD5 | NONE |
NVPTKITDCST5 | N/A |
NVPTKITDCS5 | N/A |
NVPTKITDCLT5 | N/A |
NVPTKITDCL5 | N/A |
NVPTKITC3P8T5 | N/A |
NVPTKITC3P85 | N/A |
NVPTKITC3P7T5 | N/A |
NVPTKITC3P75 | N/A |
NVPTKITC3P6T5 | N/A |
NVPTKITC3P65 | N/A |
B006NVPTST2 | N/A |
B600NVPS2 | NONE |
B600NVPMS2 | NONE |
B006NVPUSB1 | NONE |
NVPTKITDCSWF5 | NONE |
NVPTKITDCSD5 | N/A |
NVPTKITDCLWF5 | NONE |
NVPTKITDCLD5 | N/A |
NVPTKITC3P8WSF5 | N/A |
NVPTKITC3P7WSF5 | N/A |
B006NVPTKITC3P6WSF5 | N/A |
B006NVPT1 | NONE |
B006NVPSTST2 | NONE |
B006NVPMK1 | NONE |