Primary Device ID | 00850015518188 |
NIH Device Record Key | eb60d6cb-e005-4a50-8300-d1a89f110002 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NaviCam Capsule Endoscope System |
Version Model Number | Recorder/AKR-1 |
Company DUNS | 024972857 |
Company Name | ANX ROBOTICA CORP |
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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |