Primary Device ID | 06973114620300 |
NIH Device Record Key | a2839108-29d0-444f-bad0-6259576fd282 |
Commercial Distribution Discontinuation | 2056-08-18 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MEO |
Version Model Number | 17.5×9.5 |
Company DUNS | 554530265 |
Company Name | Fujian MEO Medical Technology Ltd. |
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 | true |