Primary Device ID | 00618125163977 |
NIH Device Record Key | d3cd2972-64c9-4dc1-826c-743f175a4e32 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MediDrapes Inc. |
Version Model Number | 29619 |
Company DUNS | 063519193 |
Company Name | TIDI PRODUCTS, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |