| Primary Device ID | 00840178700100 |
| NIH Device Record Key | 6ae1dd6e-387d-40e4-a612-d3e8c4a15307 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PROCARE |
| Version Model Number | 120-002407-00 |
| Company DUNS | 080434935 |
| Company Name | Touchpoint Medical, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840178700100 [Primary] |
| BZN | Cart, Emergency, Cardiopulmonary (Excluding Equipment) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-09 |
| Device Publish Date | 2024-04-01 |
| 00840178700100 | ProCare Intelligent Anesthesia Cart |
| 00840178700094 | ProCare Intelligent Procedure Cart |
| 00840178700087 | ProCare Anesthesia Cart |
| 00840178700070 | ProCare Pediatric Code Response Cart |
| 00840178700063 | ProCare Emergency Code Response Cart |
| 00840178700056 | ProCare General Procedure Cart, E-Lock |
| 00840178700049 | ProCare General Procedure Cart |
| 00840178700032 | ProCare Isolation Cart |