| Primary Device ID | 00859151005019 |
| NIH Device Record Key | 5cf903f7-750f-43a9-96ca-6a27e551dcea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MediCap |
| Version Model Number | USB300 |
| Company DUNS | 788868904 |
| Company Name | MEDICAPTURE, INC. |
| 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 | 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00859151005019 [Primary] |
| GS1 | 10859151005016 [Package] Package: [4 Units] In Commercial Distribution |
| LMD | System, Digital Image Communications, Radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-20 |
| Device Publish Date | 2020-02-12 |
| 00859151005255 | MVR400Z |
| 10859151005023 | USB170 |
| 00859151005019 | USB300 |
| 10859151005009 | USB200 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDICAP 77672145 3679253 Live/Registered |
Medicap Pharmacies Incorporated 2009-02-17 |
![]() MEDICAP 77425858 3527052 Live/Registered |
MediCapture, Inc. 2008-03-19 |
![]() MEDICAP 75049433 not registered Dead/Abandoned |
Provider Solutions, Ltd. 1996-01-29 |
![]() MEDICAP 73597721 1418011 Live/Registered |
CREATIVE SALES, INC. 1986-05-09 |