| Primary Device ID | 30641043913653 |
| NIH Device Record Key | 7c65d6d2-0052-4582-a767-96f4965bfa3c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Neo-Tee T-Piece Resuscitator Circuit |
| Version Model Number | 10-91365 |
| Company DUNS | 032705659 |
| Company Name | MERCURY ENTERPRISES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| 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 | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10641043913659 [Primary] |
| GS1 | 30641043913653 [Package] Contains: 10641043913659 Package: [10 Units] In Commercial Distribution |
| BTL | Ventilator, Emergency, Powered (Resuscitator) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-16 |
| Device Publish Date | 2024-02-08 |
| 30641043509153 | 10-50915 |
| 30641043509146 | 10-50914 |
| 30641043509054 | 10-50905 |
| 30641043509047 | 10-50904 |
| 30641043509030 | 10-50903 |
| 30641043509023 | 10-50902 |
| 30641043509016 | 10-50901 |
| 30641043509009 | 10-50900 |
| 10641043509166 | 10-50916 |
| 30641043913653 | 10-91365 |
| 30641043913356 | 10-91335 |
| 30641043913165 | 10-91316 |