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Device Explorer · FDA GUDID · GMDN 40593

Pneumatic dental power tool hose

A single- or double-lumen (coaxial) tube in a straight or spiral design intended to be used to conduct compressed gas from a source to a dental drilling system handpiece to provide power to the turbine. The device is of an adequate length to provide manoeuvrab

US‑registered devices50in commercial distribution
Companies2labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Bien-Air Portugal, Unipessoal, Lda4692%
Bien-Air Dental Sa48%

Top labelers

CompanyDevicesShare
Bien-Air Portugal, Unipessoal, Lda4692%
Bien-Air Dental Sa48%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Set MC3 LED + Hose for SironaSet MC3 LED + Hose for KavoSet MC3 LED + 4VLM-11Set MC3 LED + 4VR400 GreySet MC3 IR + 4VLM-11 GreyMC3 LK + 4VLMHOSE MX2 400 GREY_102646Hose MCX OSSTEMHOSE LIGHT MOTORHOSE MCX Grey 400 20.2x40Hose B-MCX GreyHose MCX Grey ADECTY MX2 400° calotte Ø20.2x40HOSE MX2 400 GREY 20.2x40HOSE MX2 400 SURF 6HOSE MX2 400 PLANMECA

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

FDA product codes

CodeNameDevices
EFBHandpiece, air-powered, dental46
EFBHandpiece, Air-Powered, Dental4

GMDN & GCC registration

  • GMDN code 40593 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 100% · 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

No structured size data on the register.

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

How many pneumatic dental power tool hose products are registered in the US?

50 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Pneumatic dental power tool hose", from 2 companies. The largest labeler is Bien-Air Portugal, Unipessoal, Lda with 92% of records.

Which FDA product codes apply?

EFB (Handpiece, air-powered, dental), EFB (Handpiece, Air-Powered, Dental)

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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