| Primary Device ID | B632MDB01035 |
| NIH Device Record Key | 637768d3-ada2-4ef7-96ac-31e200374037 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mediblu |
| Version Model Number | Blu15+ |
| Catalog Number | MDB01035 |
| Company DUNS | 117518078 |
| Company Name | MEDIBLU MEDICAL 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 | 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B632MDB01035 [Primary] |
| MWI | Monitor, physiological, patient (without arrhythmia detection or alarms) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-03 |
| Device Publish Date | 2020-06-25 |
| B632MDB01035 | Blu15+ |
| B632MDB01034 | BLU 12+ |
| B632MDB01028 | BLU 12 |
| B632MDB01027 | S12W |
| B632MDB01026 | S12 |
| B632MDB01024 | HP50P |
| B632MDB01023 | HA3P |
| B632MDB01013 | DVC 200 |
| B632MDB01012 | ME12P |
| B632MDB01011 | ME6P |
| B632MDB01010 | ME3 |
| B632MDB01009 | FD1 |
| B632MDB01008 | FM02 |
| B632MDB01007 | FM10 |
| B632MDB01006 | MO1 |
| B632MDB01005 | MM3 |
| B632MDB01004 | MM5 |
| B632MDB01003 | MM12 |
| B632MDB01002 | MM15 |
| B632MDB01001 | MM17 |
| B632MDB01037 | MM1 |
| B632MDB01036 | DVC 300 |
| B632MDB01038 | DVC 300 HD |
| B632MDB01040 | ME15P |
| B632MDB01042 | HA12P |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDIBLU 85404097 not registered Dead/Abandoned |
MEDIMAR, CORP. 2011-08-22 |