Primary Device ID | 00866595000227 |
NIH Device Record Key | 16ff3e7a-71a1-421e-9b4a-01f30c034a74 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Apollo Corp. |
Version Model Number | AS6300 |
Company DUNS | 098414501 |
Company Name | APOLLO CORP. |
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 | false |
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 | false |