| Primary Device ID | B5051001 |
| NIH Device Record Key | c110a493-7739-45db-9396-89e4cb7631c1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | B500 SERIES |
| Version Model Number | B505-1001 |
| Company DUNS | 959702788 |
| Company Name | BETA BIOMED SERVICES INC |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B5051001 [Primary] |
| DQA | Oximeter |
| 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 | 2016-10-18 |
| B510060203 | B500 SERIES PULSE OXIMETER SENSOR |
| B5051300 | B500 SERIES PULSE OXIMETER |
| B5051033B03 | B500 SERIES PULSE OXIMETER SENSOR |
| B505101703 | B500 SERIES PULSE OXIMETER SENSOR |
| B505101410 | B500 PULSE OXIMETER SENSOR |
| B5051014 | B500 SERIES PULSE OXIMETER SENSOR |
| B5051011N03 | B500 SERIES PULSE OXIMETER |
| B5051011M1003 | B500 SERIES PULSE OXIMETER SENSOR |
| B5051011M03 | B500 SERIES PULSE OXIMETER SENSOR |
| B5051011 | B500 SERIES PULSE OXIMETER SENSOR |
| B5051007 | B500 SERIES PULSE OXIMETER SENSOR |
| B5051005 | B500 Series Pulse Oximeter Sensor |
| B5051002N103 | B500 SERIES PULSE OXIMETER SENSOR |
| B5051002N1 | B500 PULSE OXIMETER SENSOR |
| B5051002 | B500 SPO2 PULSE OXIMETER SENSOR |
| B5051001 | B500 SERIES PULSE OXIMETER SENSOR |
| B5011011M03 | B500 SERIES PULSE OXIMETER SENSOR |
| B501100503 | B500 SERIES PULSE OXIMETER SENSOR |