| Primary Device ID | B101140100X0 |
| NIH Device Record Key | d0c47ff1-7693-494c-a654-69ca1d56869d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bolus Button Cable |
| Version Model Number | 140-100X |
| Company DUNS | 002125419 |
| Company Name | CME AMERICA LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| 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 |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx | |
| Phone | 303-936-4945 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B101140100X0 [Primary] |
| FRN | Pump, Infusion |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-15 |
| B101140100X0 | 140-100X |
| B101140000XP0 | bolus cable (1) |