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Device Explorer · FDA GUDID · GMDN 40743

Nuclear medicine system synchronizer

A physiological monitoring unit used a component of a diagnostic nuclear medicine imaging system, e.g., single photon emission computed tomography (SPECT), positron emission tomography (PET) or gamma camera, that produces a signal which enables image formation

US‑registered devices109in commercial distribution
Companies1labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Ivy Biomedical Systems, Inc.109100%

Top labelers

CompanyDevicesShare
Ivy Biomedical Systems, Inc.109100%

Company = labeler of record on GUDID. 1 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Model 7600EPModel 7600UPMM-XModel 7800EPUPMM SerialUPMMCTM-300

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

FDA product codes

CodeNameDevices
DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)110

GMDN & GCC registration

  • GMDN code 40743 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 99% · 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

Height (Inch) · 110Width (Inch) · 110Depth (Inch) · 110Weight (Pound) · 110

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

No closely related category with 50+ devices.

How many nuclear medicine system synchronizer products are registered in the US?

109 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Nuclear medicine system synchronizer", from 1 companies. The largest labeler is Ivy Biomedical Systems, Inc. with 100% of records.

Which FDA product codes apply?

DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm))

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.

How do I get quotes?

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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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