Primary Device ID | B632MDB01002 |
NIH Device Record Key | 8a10dffb-2215-4d69-a64f-b1e45bbaf798 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mediblu |
Version Model Number | MM15 |
Catalog Number | MDB01002 |
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 | B632MDB01002 [Primary] |
MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH 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 |