Primary Device ID | 09331923700472 |
NIH Device Record Key | adf0f061-0870-41c4-90b1-fd3838828ecf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ellodi |
Version Model Number | EL00003 |
Company DUNS | 543062382 |
Company Name | Shenzhen Kaiyan Medical Equipment Co,. 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 | 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 | false |
OTC Over-The-Counter | true |
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