| Primary Device ID | H671505TT1 |
| NIH Device Record Key | 32b82c4f-0a25-4fbe-a5b8-92721b38ab3d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CMI |
| Version Model Number | Ultra Cup |
| Catalog Number | 505TT |
| Company DUNS | 094651270 |
| Company Name | UTAH MEDICAL PRODUCTS, INC. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
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