Primary Device ID | 26972011720025 |
NIH Device Record Key | b470e2e6-b631-4eee-b4ca-dcd38353fbfe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EndoClot PHS |
Version Model Number | EPK2303 |
Company DUNS | 544357082 |
Company Name | EndoClot Plus 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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |