Primary Device ID | 20801741182826 |
NIH Device Record Key | 8386183b-28dc-4bec-9250-fa9036e68371 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SLP001 |
Version Model Number | SLP001 |
Catalog Number | SLP001 |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, Inc. |
Device Count | 1 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741182822 [Primary] |
GS1 | 10801741182829 [Package] Contains: 00801741182822 Package: CA [50 Units] In Commercial Distribution |
GS1 | 20801741182826 [Package] Contains: 10801741182829 Package: BX [10 Units] In Commercial Distribution |
KMK | DEVICE, INTRAVASCULAR CATHETER SECUREMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2019-01-25 |
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