Primary Device ID | 00866595000234 |
NIH Device Record Key | 0c6769b9-2f51-4e5c-9492-e46e59b0f82e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Apollo Corp. |
Version Model Number | AS7102 |
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 |