| Primary Device ID | 00850062467033 |
| NIH Device Record Key | ede2b6c2-40e0-41e9-bb5e-f9d31645857b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TMM-FC |
| Version Model Number | 05006 |
| Company DUNS | 621904622 |
| Company Name | Altitude Technologies 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 | 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 | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850062467033 [Primary] |
| OHR | Catheter Care Tray |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-11 |
| Device Publish Date | 2024-10-03 |
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