| Primary Device ID | 10748426144195 |
| NIH Device Record Key | a2346b65-64b4-40d8-b428-988efde78863 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HOLOGIC® |
| Version Model Number | Equipment Drapes |
| Catalog Number | 110788 |
| Company DUNS | 106908437 |
| Company Name | Microtek Medical LLC |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 1(800)633-5463 |
| customerservice@medline.com | |
| Phone | 1(800)633-5463 |
| customerservice@medline.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00748426144198 [Primary] |
| GS1 | 10748426144195 [Package] Contains: 00748426144198 Package: case [20 Units] In Commercial Distribution |
| PUI | Drape, Surgical, Exempt |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-12 |
| Device Publish Date | 2026-02-04 |
| 10748426144829 | MultiCare Draping System |
| 10748426144812 | Stage Draping System |
| 10748426144805 | Fischer Draping System |
| 10748426144195 | Mini C-Arm Cover |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HOLOGIC 87088681 5150254 Live/Registered |
Hologic, Inc. 2016-06-29 |
![]() HOLOGIC 86413347 4876768 Live/Registered |
Hologic, Inc. 2014-10-02 |
![]() HOLOGIC 77341464 3857248 Live/Registered |
Hologic, Inc. 2007-11-30 |
![]() HOLOGIC 74042785 1652292 Dead/Cancelled |
Hologic, Inc. 1990-03-26 |