| Primary Device ID | B101151143XL0 |
| NIH Device Record Key | b700cd6c-008b-43ff-a1f4-aa289c428866 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Wall Charger |
| Version Model Number | 151-143XL |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B101151143XL0 [Primary] |
| FRN | Pump, Infusion |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-16 |
| B101151143XLP0 | Wall Charger, Instructions |
| B101151143XL0 | 151-143XL |