| Primary Device ID | 00370858000270 |
| NIH Device Record Key | 435184ff-80d5-4e7c-84c2-3d4b2ca74fc2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SITEGUARD |
| Version Model Number | MC-SL-0008-10 |
| Company DUNS | 043989331 |
| Company Name | NEXT SCIENCE, LLC |
| Device Count | 10 |
| 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 | 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 | 00370858000263 [Unit of Use] |
| GS1 | 00370858000270 [Primary] |
| FRO | Dressing, Wound, Drug |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-03-09 |
| Device Publish Date | 2022-03-01 |
| 00370858000355 - BlastX | 2025-04-22 |
| 00370858000010 - BIOWASH Surgical Irrigation | 2024-08-08 |
| 00370858000058 - BIOWASH Surgical Irrigation | 2024-08-08 |
| 00370858000164 - TridentX | 2022-06-09 |
| 00370858000270 - SITEGUARD | 2022-03-09 |
| 00370858000270 - SITEGUARD | 2022-03-09 |
| 00370858000218 - XPERIENCE | 2021-05-06 |
| 00370858000140 - XPERIENCE | 2021-05-06 |
| 00864076000292 - Bactisure™ | 2020-12-25 |