Primary Device ID | 04048551009901 |
NIH Device Record Key | 9dd87cac-a459-4703-8c34-83cdf6c0bbda |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NAV1 |
Version Model Number | 40800060 |
Company DUNS | 315731430 |
Company Name | Karl Storz GmbH & Co. KG |
Device Count | 1 |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04048551009901 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-10-21 |
Device Publish Date | 2016-09-23 |
04048551337820 | NAV1 ELECTROMAGNETIC Field Generator |
04048551336854 | NAV1 ELECTROMAGNETIC Module |
04048551291030 | NAV1-Module |
04048551009901 | NAV1 pico Mobile Stand |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NAV1 79181139 5220210 Live/Registered |
KARL STORZ SE & Co. KG 2015-11-19 |
NAV1 79168411 5061382 Live/Registered |
KARL STORZ SE & Co. KG 2014-11-19 |