| Primary Device ID | 30382904905201 |
| NIH Device Record Key | 2a08c648-172b-4b5c-8d86-8ba074fca20e |
| Commercial Distribution Discontinuation | 2015-08-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | PrepStain® Settling Chambers |
| Version Model Number | 490520 |
| Catalog Number | 490520 |
| Company DUNS | 103318015 |
| Company Name | TRIPATH IMAGING, INC. |
| Device Count | 96 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | 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 | 00382904905201 [Unit of Use] |
| GS1 | 30382904905201 [Primary] |
| MKQ | Processor, Cervical Cytology Slide, Automated |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-05-05 |
| 10382904905245 - ROVERS® CERVEX-BRUSH® | 2019-04-05 ROVERS® CERVEX-BRUSH® |
| 10382904905269 - Rovers ® Combo-brush® | 2019-04-05 Rovers ® Cervex-Brush® Combi |
| 10382904912533 - BD SurePath™ Collection Vial Kit 500 | 2019-04-05 BD SurePath™ Collection Vial Kit 500: BD SurePath™ Collection Vials (500) |
| 30382904913244 - BD SurePath™ Collection Vial Kit 25 | 2019-04-05 BD SurePath™ Collection Vial Kit 25 |
| 30382904913299 - BD Settling Chambers | 2019-04-05 BD Settling Chambers (96). Consumables for use on the PrepStain instrument. |
| 30382904913305 - BD Settling Chambers | 2019-04-05 BD Settling Chambers |
| 00382904912475 - BD SurePath | 2019-04-05 BD SurePath™ GYN Cytology Test Kit |
| 00382904913069 - BD Density Reagent | 2019-04-05 BD Density Reagent (1900mL) |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PREPSTAIN 76341485 3002232 Live/Registered |
TriPath Imaging, Inc. 2001-11-19 |