| Primary Device ID | 00026072025055 |
| NIH Device Record Key | 5bd2c681-6108-4188-b6a5-b58b292ed35c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GM |
| Version Model Number | 01-90-8830 |
| Company DUNS | 119066872 |
| Company Name | Allied Medical, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Manufacturing Date | false |
| 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 |