| Primary Device ID | 00801741086939 |
| NIH Device Record Key | fb986993-6be3-47eb-a15b-2b0bd4b21073 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SITE-SCRUB |
| Version Model Number | 3882025 |
| Company DUNS | 044611812 |
| Company Name | Bard Access Systems, Inc. |
| Device Count | 25 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741086939 [Unit of Use] |
| GS1 | 10801741086936 [Primary] |
| LKB | Pad, alcohol, device disinfectant |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-21 |
| Device Publish Date | 2023-12-13 |
| 00801741086946 | Site-ScrubTM IPA Device |
| 00801741086939 | Site-ScrubTM IPA Device |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SITE-SCRUB 77526601 3990406 Live/Registered |
BARD ACCESS SYSTEMS, INC. 2008-07-19 |