Primary Device ID | 00810143451221 |
NIH Device Record Key | 057a65df-75c7-44a4-ba48-7fa3ba375145 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EndoGuidance L-Hook Electrode |
Version Model Number | MDPL-33 |
Company DUNS | 961673774 |
Company Name | Medical Disposables 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 | 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 |