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 |