SLP001 SLP001

GUDID 20801741182826

StatLock Pro, single

Bard Access Systems, Inc.

Wearable percutaneous catheter/tube holder
Primary Device ID20801741182826
NIH Device Record Key8386183b-28dc-4bec-9250-fa9036e68371
Commercial Distribution StatusIn Commercial Distribution
Brand NameSLP001
Version Model NumberSLP001
Catalog NumberSLP001
Company DUNS044611812
Company NameBard Access Systems, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100801741182822 [Primary]
GS110801741182829 [Package]
Contains: 00801741182822
Package: CA [50 Units]
In Commercial Distribution
GS120801741182826 [Package]
Contains: 10801741182829
Package: BX [10 Units]
In Commercial Distribution

FDA Product Code

KMKDEVICE, INTRAVASCULAR CATHETER SECUREMENT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-07-22
Device Publish Date2019-01-25

Devices Manufactured by Bard Access Systems, Inc.

10801741238830 - PowerPICC Provena SOLO2026-02-19 Catheter Placement Kit
00801741038464 - Niagara Slim-Cath catheter2026-02-05 12Fr Niagara PC 15cm Kit
00801741038471 - Niagara Slim-Cath Catheter2026-02-05 12Fr Niagara PC 20cm Kit
00801741038488 - Niagara Slim-Cath catheter2026-02-05 12Fr Niagara PC 24cm Kit
00801741045141 - Niagara Slim-Cath catheter2026-02-05 12 Fr Niagara PC 12.5 cm Kit
00801741045158 - Niagara Slim-Cath catheter2026-02-05 12Fr Niagara PC 15cm Kit
10801741231275 - CentroVena One2026-02-02 CentroVena One™ Insertion System Central Venous Catheter
10801741231282 - CentroVena One2026-02-02 CentroVena One™ Insertion System Central Venous Catheter

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.