| Primary Device ID | 00817051022970 |
| NIH Device Record Key | 714ef112-f380-4aa7-bc26-7d69ef9444f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | StatStix |
| Version Model Number | 380065 |
| Company DUNS | 053707303 |
| Company Name | CENTRIX, INC. |
| Device Count | 1 |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817051022970 [Primary] |
| MVL | Cord, Retraction |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-08 |
| Device Publish Date | 2023-12-29 |
| 00817051022970 | StatStix Black Regular |
| 00817051022963 | StatStix Red Fine |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() STATSTIX 97016632 not registered Live/Pending |
Centrix, Inc. 2021-09-08 |
![]() STATSTIX 87683465 not registered Live/Pending |
Centrix, Inc. 2017-11-14 |