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Device Lab 3

PET/CT

PET/CT in the BMEssentia 3D Device Lab

The scanner housing joins two measurement systems around one patient pathway. The front station contains CT; the PET ring sits behind it.

Also called: Pet Scanner, Positron Emission Tomography. Arabic: التصوير المقطعي بالإصدار البوزيتروني. Device Lab 3 of 69 in BMEssentia Medical City, 2 configurations.

How it works: the main parts

What each part does, from the PET/CT lessons in the 3D Device Lab.

CT acquisition assembly
CT measures how an external X-ray beam is attenuated through the patient. Its source and opposing detector array rotate around the bore.
PET detector ring
The PET ring surrounds the patient with many detector modules. Each module contributes measurements; no single block produces the final image.
Scintillator crystals
The scintillator is where deposited gamma energy becomes light. A PET photon can interact in the crystal and produce a short flash too small and fast to see directly.
Silicon photomultipliers
The silicon photomultiplier converts the scintillator flash into an electrical signal. It contains many tiny avalanche cells that respond to incoming light.
Timing and energy readout
Readout electronics turn a pulse into estimates of energy, arrival time and channel location. Those estimates decide whether an event is useful.
Coincidence processor
The coincidence processor compares detections and accepts pairs that satisfy the acquisition conditions. A pair can be consistent with one annihilation, but timing agreement alone cannot prove that both photons came from the same event.
Patient support and drive
The patient support establishes the moving coordinate system shared by PET and CT. The narrow top, drive and position feedback work together.
Positioning controls
The gantry controls let the technologist position the support while watching the patient. Their location matters: a control is useful only when the operator can see the movement and reach the relevant stop or adjustment.

Explore it in the Device Lab

Common faults and what to check

Guided fault cases in the Device Lab

Training cases written by BMEssentia for teaching.

Most reported device problems (FDA MAUDE)

Device problemReports
Nonstandard Device89
Unintended System Motion81
Loose or Intermittent Connection74
Component Falling73
Device Operates Differently Than Expected56
Mechanical Problem53

Raw counts of adverse event reports for this device type (FDA product code KPS), all years. Not adjusted for the number of units in use, so they show what gets reported, not failure rates. Report text is never copied.

Planned maintenance checks

From the BMEssentia procedure library: every 12 months, about 240 minutes, electrical class I, applied part type B.

CT part as for the CT scanner. PET quality control follows the manufacturer and NEMA NU 2 at acceptance; daily QC uses the manufacturer's source.

CheckPass when
Gantry, table and room
Inspect the gantry, table, lasers, the hot lab shielding and warning signs.
No damage; signs in place.
Electrical safety
Test table and accessories to IEC 62353.
Within limits.
PET QC and SUV
Review daily QC trends; scan the uniform phantom and compare SUV.
Within the manufacturer's limits and SUV tolerance.
Registration and CT
Check PET/CT registration with the manufacturer's test; CT checks as for the CT scanner.
Within tolerance.

Test instruments: Manufacturer's daily QC source; NEMA NU 2 phantom (acceptance and annual, physics); Dose calibrator (radiopharmacy).

Recent FDA recalls

RecallProduct and reason
Z-3283-2026
2026-09-25
Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System, Model: uMI 550 with software
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from. Root cause: Software design.
Z-3284-2026
2026-09-25
Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System, Model: uMI Panorama 35 with software
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from. Root cause: Software design.
Z-3285-2026
2026-09-25
Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System, Model: uMI Panorama GS with software
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from. Root cause: Software design.
Z-3286-2026
2026-09-25
Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo with software
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from. Root cause: Software design.
Z-3287-2026
2026-09-25
Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System, Model: uMI Panvivo S with software
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from. Root cause: Software design.

From the FDA recall database (openFDA), newest first, imported 2026-10-22. 208 recalls on record for this device type. Recall text is the FDA's public text; each recall links to the official record.

Learn it, see it in 3D, ask about it

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