| Primary Device ID | B631DLSGPHP5PL13F1 |
| NIH Device Record Key | ae6d60ec-a4d0-4fc3-9c9a-c2aff58105ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SureLead |
| Version Model Number | DLSGPHP5PL13F |
| Company DUNS | 078861998 |
| Company Name | Authentic Medical |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B631DLSGPHP5PL13F1 [Primary] |
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-15 |
| Device Publish Date | 2022-09-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SURELEAD 98844045 not registered Live/Pending |
Authentic Options LLC 2024-11-08 |