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 |