Primary Device ID | 00841439102053 |
NIH Device Record Key | cbfbfafa-6241-4750-9e42-806b17f64bcd |
Commercial Distribution Discontinuation | 2019-05-02 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Grid Panel |
Version Model Number | 20IL430003 |
Catalog Number | 20IL430003 |
Company DUNS | 103977526 |
Company Name | MEDTEC, INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 | true |
OTC Over-The-Counter | false |