Stryker High Flow 40-Liter Insufflator
Stryker · Model High Flow 40-Liter Insufflator
• The highest flow rate available on the market • Neonatal mode offers increased sensitivity and floew rates as low as .1 liters per minute • LCD display provides surgeons with ongoing status messages • Sidne compatibility allows the surgeon to control the insufflator with voice commands • Software driven to allow for future upgrades • Built in gas heating technology • Video on-screen display Safety • Surgivent-electronic venting system for added safety • Visual and audible warning signals • Safety Relief Value • Internal Leakage Detection
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
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Insertion tube / bending wear
HighSymptoms: Stiff angulation, image artifacts.
Root cause: Repeat flexing / reprocessing.
Leak (water ingress)
HighSymptoms: Fogging, failed leak test.
Root cause: Damaged outer sheath.
Image sensor / CCD fault
HighSymptoms: No/poor image, color error.
Root cause: Sensor or cable failure.
Channel blockage
MediumSymptoms: Poor suction / irrigation.
Root cause: Debris in working channel.
Serviceable Parts & Consumables
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
Working channel liner
Class Periodic replacementRel. cost $$$R&R Difficult
Outer sheath / distal end
Class Periodic replacementRel. cost $$$$R&R Expert-level
Angulation cable / mesh
High-value R&R.
Class Periodic replacementRel. cost $$$$R&R Expert-level
Image sensor module
Class Periodic replacementRel. cost $$$$R&R Expert-level
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Working channel liner | Periodic replacement | $$$ | Difficult |
| Outer sheath / distal end | Periodic replacement | $$$$ | Expert-level |
| Angulation cable / mesh High-value R&R. | Periodic replacement | $$$$ | Expert-level |
| Image sensor module | Periodic replacement | $$$$ | Expert-level |
Relative cost: $ lowest · $$$$ 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 structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: Insertion tube / bending wear
- Confirm the presentation - typically stiff angulation, image artifacts - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: repeat flexing / reprocessing.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the angulation cable / mesh per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Symptom: Image sensor / CCD fault
- Confirm the presentation - typically no/poor image, color error - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: sensor or cable failure.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the image sensor module per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Technical Specs
- Height
- 5.83 in
- Length
- 18.7 in
- Weight
- 19.84 lbs
- Width
- 12.52 in
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
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
Potential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the ACM system and bio-incompatibility due to components falling into surgical site
- RECALL
Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, may lead to operative site blood loss, hemorrhage or, in exceedingly rare situations, other major complications
- RECALL
There is a potential for the cuff to leak air leading to a loss of vascular occlusion.
- RECALL
The heated tube sets were consistently leaking and detaching from the cassette.
- RECALL
Issue with the process for detection of leaking Pressure Tourniquet Cuffs (PTC). Leaking PTC devices may result in excessive blood loss requiring surgical or medical intervention or systemic leakage of local anesthetic during Bier Block requiring medical intervention.
- RECALL
Stryker Neurovascular has become aware that some units of Target Nano product do not have the intended stretch resistance. The sutures inside the coil that provide stretch resistance may have been damaged during manufacturing which can lead to an increased occurrence of coil stretching.
- RECALL
When operating the device in high flow mode (40L/min, 15 mmHg) and connecting to a house gas inlet source, within seconds of insufflating the flow rate would drop to 0L/min and the red Check Gas Supply symbol would appear on the display, immediately suspending insufflation.
- RECALL
Sterility may be compromised, as the packaging may have channels in the packaging seal.
- RECALL
Device for which sterility may be compromised as evidenced by a loss of package integrity.
- RECALL
Non-sterilized product sold as sterile.
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