| Primary Device ID | 05391536710002 |
| NIH Device Record Key | c57d2111-3545-4e7f-8f7e-93cbaac3c1e8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bluedrop Medical |
| Version Model Number | 05391536710002 |
| Company DUNS | 985593930 |
| Company Name | BLUEDROP MEDICAL LIMITED |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05391536710002 [Primary] |
| OIZ | Foot Examination Tool For Inflammatory Changes |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-26 |
| Device Publish Date | 2023-09-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BLUEDROP MEDICAL 98045235 not registered Live/Pending |
Bluedrop RPM, Inc. 2023-06-15 |