Jiyuan
Jiangsu Jiyuan Medical Technology Co .,Ltd. · Model JY-MIP-1000
CVBS/HDMI, ARMI, Image processor for medical endoscope.
Intended use: An electrically-powered device designed to receive and process the electronic signals sent from a video endoscope or endoscopic video camera; it does not include the endoscope nor light source and is not designed to control the endoscope. It may have additional features which compensate for/enhance the colour and light qualities provided. The resulting picture images are sent to and shown on a visual display unit (VDU), typically to assist the endoscope operator with an ongoing intervention and often to allow the patient visualization of the process; the images can be recorded on a video recorder or stored on computerized media.
Key tips
- ·A failed leak test means the scope does not get reprocessed or used - send it for repair, full stop.
- ·A shortened reprocessing cycle is a real infection-control failure, not a minor deviation - follow AAMI ST91 exactly.
- ·Track light-source lamp-hours against the manufacturer's limit rather than running to failure.
Typical Failure Modes
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
No or inconsistent X-ray exposure
HighSymptoms: No exposure on the hand-switch, error code, images under- or over-exposed.
Root cause: Depleted battery, a hand-switch / exposure-relay fault, or an X-ray tube / HV generator fault.
Battery / powered-drive fault
HighSymptoms: Few exposures per charge, the powered drive is weak or dead, will not charge.
Root cause: Aged battery pack or a drive-motor / charger fault.
Poor image quality
MediumSymptoms: Blurry, noisy or low-contrast images despite correct technique.
Root cause: Tube focal-spot degradation, generator instability, or the DR detector / wireless link.
Collimator / positioning-arm fault
MediumSymptoms: Collimator light out, arm drifts or will not hold position.
Root cause: Collimator lamp, or worn arm friction / counterbalance.
Serviceable Parts & Consumables
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
Battery pack
Class Frequent wear itemRel. cost $$R&R Fairly easy
X-ray tube / HV generator assembly
Class Major service partRel. cost $$$$R&R Expert-level
Hand-switch / exposure relay
Class Periodic replacementRel. cost $$R&R Moderate
Collimator lamp
Class Periodic replacementRel. cost $R&R Fairly easy
Positioning-arm friction / counterbalance kit
Class Major service partRel. cost $$R&R Moderate
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Battery pack | Frequent wear item | $$ | Fairly easy |
| X-ray tube / HV generator assembly | Major service part | $$$$ | Expert-level |
| Hand-switch / exposure relay | Periodic replacement | $$ | Moderate |
| Collimator lamp | Periodic replacement | $ | Fairly easy |
| Positioning-arm friction / counterbalance kit | Major service part | $$ | Moderate |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
PM Checklist
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
- ·Leak testing before each reprocessing cycle
- ·Scope reprocessing per AAMI ST91
- ·Light source lamp-hour tracking
- ·Annual full PM
Troubleshooting Approach
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Symptom: No exposure
- Confirm a charged battery and the exposure count per charge.
- Check the hand-switch and any interlock.
- Note the exact error code.
- Let the tube cool if a thermal lockout is active.
- Escalate a confirmed tube / generator fault to the manufacturer.
Symptom: Poor image quality
- Confirm technique (kV / mAs) for the study.
- Check the DR detector / wireless link and calibration.
- Compare against a phantom exposure.
- Escalate tube focal-spot degradation to the manufacturer.
- Verify with a repeat phantom image.
Technical Specs
- MRI safety
- Labeling does not contain MRI Safety Information
- Sterile
- Yes
- Single use
- Yes
- Prescription use
- OTC
- FDA distribution status
- In Commercial Distribution
- Device type (GMDN)
- Endoscopic video image processing unit
- FDA product classification
- Hysteroscope (And Accessories)
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Endoscopy suite / GI lab
- Operating Room
- Bronchoscopy suite
Documents & Manuals
No documents available for this device yet.
Troubleshoot this device with Bio
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio