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Device Explorer · FDA GUDID · GMDN 61142

Vascular access device flush/disinfection tool

A manual device intended to be used to flush wash the lumen of an in situ vascular access device (e.g., catheter, needleless intravenous line) and to disinfect the device’s Luer access valve. It consists of a prefilled syringe containing a saline solution, and

US‑registered devices101in commercial distribution
Companies7labelers on GUDID
Single‑use100%of device records
Sterile84%labelled sterile
Prescription96%Rx‑only share
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Share of device records

Medical Action Industries Inc.8180%
Medline Industries, Inc.1111%
O&M Halyard, Inc.44%
Resource Optimization & Innovation, L.L.C.22%
Bound Tree Medical, Llc11%
Becton, Dickinson And Company11%
Owens & Minor Distribution, Inc.11%

Top labelers

CompanyDevicesShare
Medical Action Industries Inc.8180%
Medline Industries, Inc.1111%
O&M Halyard, Inc.44%
Resource Optimization & Innovation, L.L.C.22%
Bound Tree Medical, Llc11%
Becton, Dickinson And Company11%
Owens & Minor Distribution, Inc.11%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CuraplexBD PosiFlush SafeScrubRegard™PENDINGMedichoiceMEDICAL ACTION INDUSTRIESClear SequenceMedical Action IndustriesMAImedical Action IndustriesAVID TRUCUSTOMInfuSystem®HalyardExcelsior

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
PEZCentral venous catheter dressing change kit133
OFFCentral venous catheter tray118
LROGeneral surgery tray17
NGTSaline, vascular access flush16
OWLPeripheral catheter insertion kit3
OFDCatheter introducer kit2

GMDN & GCC registration

  • GMDN code 61142 · non‑implantable
  • Single‑use 100% · sterile 84% · Rx‑only 96% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Total Volume (Milliliter) · 8Needle Gauge (Gauge) · 1Length (Centimeter) · 1

Use these as the dimensions to specify in a tender line.

How many vascular access device flush/disinfection tool products are registered in the US?

101 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vascular access device flush/disinfection tool", from 7 companies. The largest labeler is Medical Action Industries Inc. with 80% of records.

Which FDA product codes apply?

PEZ (Central venous catheter dressing change kit), OFF (Central venous catheter tray), LRO (General surgery tray), NGT (Saline, vascular access flush)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

How do I get quotes?

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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