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Device Explorer · FDA GUDID · GMDN 38437

Brachytherapy system remote afterloading source transfer tube

A tube or hose-like catheter with connectors at both ends used to interface the brachytherapy applicator to the remote afterloading system. The transfer tube, when attached to the applicator and the afterloading system, provides a continuous closed passage tha

US‑registered devices594in commercial distribution
Companies3labelers on GUDID
Single‑use1%of device records
Sterile0%labelled sterile
Prescription16%Rx‑only share
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Share of device records

Nucletron B.V.50084%
Varian Medical Systems Deutschland Gmbh8414%
Varian Medical Systems, Inc.102%

Top labelers

CompanyDevicesShare
Nucletron B.V.50084%
Varian Medical Systems Deutschland Gmbh8414%
Varian Medical Systems, Inc.102%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

X-ray marker BV set II, up to 500 mm tubes, codeX-ray marker BV set I, up to 500 mm tubes, codedX-ray marker BV set Intraluminal, up to 1300 mm X-ray marker BV set II, up to 200 mm needles, coX-ray marker BV set I, up to 200 mm needles, codX-ray marker BV set II, up to 320 mm applicatorsX-ray marker BV set I, up to 320 mm applicators,X-ray marker BV, up to 1300 mm catheters, uncodeX-ray marker BV, up to 320 mm applicators, uncodLength Gauge, GammaMedplusLength Assessment DeviceTransfer Guide Tube, 1000 mm length for catheterTransfer Guide Tube for 500 mm cathetersTransfer Guide Tube for 320 mm cathetersTransfer Guide Tube for 250 mm cathetersTransfer Guide Tube for 200 mm catheters

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

FDA product codes

CodeNameDevices
JAQSystem, applicator, radionuclide, remote-controlled662
JAQSystem, Applicator, Radionuclide, Remote-Controlled7

GMDN & GCC registration

  • GMDN code 38437 · non‑implantable
  • Single‑use 1% · sterile 0% · Rx‑only 16% · 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 (Millimeter) · 25Catheter Gauge (French) · 1

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

No closely related category with 50+ devices.

How many brachytherapy system remote afterloading source transfer tube products are registered in the US?

594 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Brachytherapy system remote afterloading source transfer tube", from 3 companies. The largest labeler is Nucletron B.V. with 84% of records.

Which FDA product codes apply?

JAQ (System, applicator, radionuclide, remote-controlled), JAQ (System, Applicator, Radionuclide, Remote-Controlled)

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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