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Device Explorer · FDA GUDID · GMDN 60417

Luer/non-ISO80369-standardized linear connector, reusable

A small, non-powered, noninvasive, tubular, two-way/linear connector with a Luer connection (either lock or slip) at one end and a connection which is not designed according to ISO 80369 (standard for small-bore connectors for liquids and gases) at the other e

US‑registered devices90in commercial distribution
Companies18labelers on GUDID
Single‑use10%of device records
Sterile0%labelled sterile
Prescription87%Rx‑only share
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Share of device records

Karl Storz Gmbh & Co. Kg4044%
Medivators Inc.1011%
Ace Surgical Supply Co., Inc.910%
Avalign Technologies, Inc.78%
Richard Wolf Gmbh67%
Hoya Corporation22%
Pentax Medical Corporation22%
Gimmi Gmbh22%

Top labelers

CompanyDevicesShare
Karl Storz Gmbh & Co. Kg4044%
Medivators Inc.1011%
Ace Surgical Supply Co., Inc.910%
Avalign Technologies, Inc.78%
Richard Wolf Gmbh67%
Hoya Corporation22%
Pentax Medical Corporation22%
Gimmi Gmbh22%
Aesculap Ag22%
Atricure, Inc.22%
Nobel Biocare Ab11%
Olympus Winter & Ibe Gmbh11%

Company = labeler of record on GUDID. 18 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NAPENTAXPENTAX MedicalERAGONTIPCONTROLGimmin.a.MIP Minimal Invasive PCNLELAN 4OlympusGen. Acces/ Instr. Tip GuardASSILUX Expandable Interbody SystemLiV™ InstrumentsDual check valveScope Buddy Plus Blanking Cap

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

FDA product codes

CodeNameDevices
FDFColonoscope and accessories, flexible/rigid21
MNLACCESSORIES, CLEANING BRUSHES, FOR ENDOSCOPE14
FEBAccessories, Cleaning, For Endoscope12
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT9
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE6
ODGEndoscopic ultrasound system, gastroenterology-urology4

GMDN & GCC registration

  • GMDN code 60417 · non‑implantable
  • Single‑use 10% · sterile 0% · Rx‑only 87% · OTC 1%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 1

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

How many luer/non-iso80369-standardized linear connector, reusable products are registered in the US?

90 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Luer/non-ISO80369-standardized linear connector, reusable", from 18 companies. The largest labeler is Karl Storz Gmbh & Co. Kg with 44% of records.

Which FDA product codes apply?

FDF (Colonoscope and accessories, flexible/rigid), MNL (ACCESSORIES, CLEANING BRUSHES, FOR ENDOSCOPE), FEB (Accessories, Cleaning, For Endoscope), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT)

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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