| Primary Device ID | B16556620326113024149 |
| NIH Device Record Key | c548bb1e-0c00-47e1-8ff2-43988dd1557f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Intrauterine Tandem |
| Version Model Number | 5662 |
| Company DUNS | 967592978 |
| Company Name | Liberty Medical , Inc. |
| 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 | 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B16556620326113024149 [Primary] |
| IWJ | System, Applicator, Radionuclide, Manual |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-18 |
| Device Publish Date | 2024-11-08 |
| B16559250325063023079 | Intrauterine tandem, 6mm OD, graduated |
| B16556620325033123048 | Intrauterine tandem, 6mm OD, graduated |
| B16556620325033123035 | Intrauterine tandem, 6mm OD, graduated |
| B16556620325123123088 | Intrauterine tandem, 6mm OD, graduated |
| B16559250326033123186 | Intrauterine tandem, 6mm OD, graduated |
| B16559250326043024046 | Intrauterine tandem, 6mm OD, graduated |
| B16556620326073123211 | Intrauterine tandem, 6mm OD, graduated |
| B16559250326083124049 | Intrauterine tandem, 6mm OD, graduated |
| B16556620326113024149 | Intrauterine tandem, 6mm OD, graduated |
| B165592503270131240431 | Intrauterine tandem, 6mm OD, graduated |