Consulting Wallah › Device Explorer › Other devices › Luminal device flushing tubing set, reusable
Device Explorer · FDA GUDID · GMDN 61723

Luminal device flushing tubing set, reusable

A collection of devices which includes connection tubing intended to be fitted to a luminal device (e.g., catheter, endoscope channel, ophthalmic handpiece) to assist flushing the device lumen during a medical/surgical procedure, and/or to assist the washing,

US‑registered devices632in commercial distribution
Companies12labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription22%Rx‑only share
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Share of device records

Steris Corporation22536%
Medivators Inc.19931%
Olympus Medical Systems Corp.9615%
Pentax Of America, Inc.416%
Corporation Steris Canada406%
Fujifilm Corporation112%
Nakanishi Inc.102%
Hoya Corporation30%

Top labelers

CompanyDevicesShare
Steris Corporation22536%
Medivators Inc.19931%
Olympus Medical Systems Corp.9615%
Pentax Of America, Inc.416%
Corporation Steris Canada406%
Fujifilm Corporation112%
Nakanishi Inc.102%
Hoya Corporation30%
Pentax Medical Corporation30%
Schölly Fiberoptic Gmbh20%
Geuder Aktiengesellschaft10%
Trulife Limited10%

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

Brand names on the register (sample)

N/APENTAX MedicalPENTAXCONNECTING TUBEAUXILIARY WATER INLET CAPAW channel cleaning adapteSuction cleaning adapterCap chainETO CAPSuction cleaning adaptorWASHING TUBEALL-CHANNEL IRRIGATORWater-resistant capInjection tubeChannel plugWATER RESISTANT CAP

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

FDA product codes

CodeNameDevices
FEBAccessories, cleaning, for endoscope369
MEDSterilant, medical devices168
PUPEndoscope maintenance system79
FEBAccessories, Cleaning, For Endoscope52
NVEWasher, cleaner, automated, endoscope34
ITXTransducer, ultrasonic, diagnostic19

GMDN & GCC registration

  • GMDN code 61723 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 22% · OTC 26%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

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

No closely related category with 50+ devices.

How many luminal device flushing tubing set, reusable products are registered in the US?

632 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Luminal device flushing tubing set, reusable", from 12 companies. The largest labeler is Steris Corporation with 36% of records.

Which FDA product codes apply?

FEB (Accessories, cleaning, for endoscope), MED (Sterilant, medical devices), PUP (Endoscope maintenance system), FEB (Accessories, Cleaning, For Endoscope)

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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