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 |