Consulting Wallah › Device Explorer › Other devices › Luer/Luer linear connector, single-use
Device Explorer · FDA GUDID · GMDN 60538

Luer/Luer linear connector, single-use

A small, non-powered, noninvasive tubular, two-way/linear connector with a Luer connection (either lock or slip) at both ends intended to connect two luminal devices (e.g., catheter, tubing, container) with each other. It may have a straight or elbow shape; it

US‑registered devices194in commercial distribution
Companies31labelers on GUDID
Single‑use99%of device records
Sterile97%labelled sterile
Prescription85%Rx‑only share
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Share of device records

Icu Medical, Inc.5428%
Becton, Dickinson And Company2613%
Teleflex Incorporated179%
Bioseal147%
Cook Incorporated126%
International Medical Industries Inc.84%
B. Braun Medical Inc.63%
Epimed International, Inc63%

Top labelers

CompanyDevicesShare
Icu Medical, Inc.5428%
Becton, Dickinson And Company2613%
Teleflex Incorporated179%
Bioseal147%
Cook Incorporated126%
International Medical Industries Inc.84%
B. Braun Medical Inc.63%
Epimed International, Inc63%
Medtronic, Inc.63%
Codan Us Corporation53%
Bd Switzerland Sàrl42%
Epic International(Thailand) Company Limited42%

Company = labeler of record on GUDID. 31 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

FlexTubeTRUWAVEHemo Luer LockIMEDULTRASITE®INT StopperConnectorFluid Dispensing ConnectorFilter HubICU MedicalLumiGuideADDTOiLet Connect Adapter 15-Pack (BB3052)iLet Connect AdapterHealth Care Logistics, Inc®COOK

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

FDA product codes

CodeNameDevices
FPASet, administration, intravascular44
GCDCONNECTOR, CATHETER18
FPASet, Administration, Intravascular14
GCYAPPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED13
DTLAdaptor, stopcock, manifold, fitting, cardiopulmonary bypass9
FMINeedle, hypodermic, single lumen9

GMDN & GCC registration

  • GMDN code 60538 · non‑implantable
  • Single‑use 99% · sterile 97% · Rx‑only 85% · 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

Length (Inch) · 17Total Volume (Milliliter) · 6Catheter Gauge (French) · 6Length (Millimeter) · 2Lumen/Inner Diameter (Inch) · 2

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

How many luer/luer linear connector, single-use products are registered in the US?

194 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Luer/Luer linear connector, single-use", from 31 companies. The largest labeler is Icu Medical, Inc. with 28% of records.

Which FDA product codes apply?

FPA (Set, administration, intravascular), GCD (CONNECTOR, CATHETER), FPA (Set, Administration, Intravascular), GCY (APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED)

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.

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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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