Primary Device ID | 00801741224676 |
NIH Device Record Key | 220e2ad1-a17b-48b6-bf1f-269d15e83b7e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sherlock 3CG+ TCS SR Halcyon SW Version 3.1.0 |
Version Model Number | S3CG+ TCS SR Halcyon SW v3.1.0 |
Catalog Number | S3CG+ TCS SR Halcyon SW v3.1.0 |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, 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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741224676 [Primary] |
LJS | Catheter, intravascular, therapeutic, long-term greater than 30 days |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-17 |
Device Publish Date | 2022-05-09 |
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