Kimberly-Clark PMG-115-TD
Kimberly-Clark · Model PMG-115-TD
Lightweight and portable Context sensitive settings Only relevant settings are displayed and active for each mode Large, clear LCD screen Real-time digital and graphical display of critical treatment data including temperature, time, power or voltage, and impedance Mode selection Soft-touch keys for selection of available modes Single on/off switch Button illuminates when output is on Intelligent probe recognition Generator identifies probe and displays only relevant information for each mode.
Key tips
- ·Most "no output" stim-unit complaints are cable-side - check electrode/lead continuity before assuming a unit fault.
- ·Frame and strap wear on mechanical rehab equipment is a real fall/injury risk - don't defer it as cosmetic.
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 low output on a modality / channel
HighSymptoms: Ultrasound, e-stim, shortwave or laser channel delivers no or weak output, error on that channel, patient feels nothing.
Root cause: Applicator / electrode / handpiece fault, a lead / cable fault, dried electrodes, or an output-stage fault on that module.
Therapeutic-ultrasound applicator fault
MediumSymptoms: Low or no ultrasound output, applicator-contact / BNR error, no warmth on a water-bath test.
Root cause: Worn or cracked applicator crystal, or a cable fault.
Electrode / lead-wire wear
MediumSymptoms: Intermittent stim, open-circuit error, uneven sensation.
Root cause: Worn lead wires or exhausted / dried self-adhesive electrodes.
Touchscreen / control fault
MediumSymptoms: Unresponsive or erratic touchscreen, parameters will not set.
Root cause: Touchscreen or controller fault.
Power / battery / cooling fault
LowSymptoms: Will not power on, short battery life, or shuts down on temperature.
Root cause: Power supply / fuse, an aged battery, or a cooling-fan fault.
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.
Therapeutic-ultrasound applicator
Class Periodic replacementRel. cost $$R&R Easy
Electrotherapy lead wires
Class Frequent wear itemRel. cost $R&R Easy
Self-adhesive / carbon electrodes
Class ConsumableRel. cost $R&R Easy
Output board / module
Class Major service partRel. cost $$$R&R Difficult
Touchscreen / control assembly
Class Major service partRel. cost $$R&R Moderate
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Therapeutic-ultrasound applicator | Periodic replacement | $$ | Easy |
| Electrotherapy lead wires | Frequent wear item | $ | Easy |
| Self-adhesive / carbon electrodes | Consumable | $ | Easy |
| Output board / module | Major service part | $$$ | Difficult |
| Touchscreen / control assembly | Major service part | $$ | 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.
- ·Frame and strap wear inspection
- ·Electrode lead continuity check
- ·Annual electrical safety test
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 or low output on a modality / channel
- Fit a fresh applicator / handpiece / electrodes for that modality.
- Substitute a known-good lead / cable.
- Test therapeutic-ultrasound output into a water bath (visible cavitation / warmth) and run the applicator-contact / BNR self-test.
- Try the modality on another unit if available.
- Escalate a confirmed output-stage fault to the OEM.
Symptom: Patient feels nothing / open-circuit on an e-stim channel
- Fit fresh self-adhesive electrodes on well-prepped skin.
- Swap the lead wires.
- Confirm the current ramps and there is no open-electrode alarm.
- Test the channel into a resistive load per the manual.
- Refer the output stage if a good lead set still gives nothing.
Symptom: Unresponsive or erratic touchscreen / parameters will not set
- Power-cycle the unit.
- Recalibrate / re-seat the touchscreen if the touch is offset.
- Check the mains fuse and power supply.
- Confirm the cooling fan runs and the vents are clear.
- Replace the touchscreen or power supply as isolated.
Technical Specs
- Neuromuscular Electrical Stimulation (NMES)
- YES
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Physical therapy / rehab gym
- Outpatient rehab clinic
- Sports medicine
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.
- RECALL
Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7 mL Epilor plastic Luer-Lok LOR Syringes under recall by Becton Dickinson (BD) because the product may stall or stick when traveling within the barrel of the syringe.
- RECALL
A defect of the "fuse holder" can lead to a Control Unit failure that may cause the device to lose its ability to warm and maintain set temperature and may also result in excessive heat with the fuse assembly that could lead to the generation of smoke.
- RECALL
The product is misbranded, i.e. the Gastric (center) port may be mislabeled as the Jejunal port, and the Jejunal (side) port mislabeled as the Gastric port.
- RECALL
A limited number of Kotex Natural Balance Security Unscented Tampons, regular absorbency, are being recalled after a raw material contaminated with a bacterium, Enterobacter sakazakii, was found when testing the plunger portion of the applicator.
- RECALL
Metal shavings were found within the folded portion of the surgical drape.
- RECALL
The impacted product was not intended for commercial distribution to end users.
- RECALL
Error 85 alarm on the Model 1000 Control Unit was occasionally triggered inappropriately.
- RECALL
The placement guidewire diameter is too large and does not pass-through the introducer needle during the placement procedure of the PEG Feeding Tube.
- RECALL
Complaints were received of gowns pilling or balling, linting and abrades, blood strikethrough and fibers falling off the gowns.
- RECALL
The product may contain defects/holes reducing the product's effectiveness as a barrier.
- RECALL
The tubes may kink during use which may impede or prevent ventilation.
- RECALL
The tinfoil in the triangle electrodes has the potential to develop cracks which may hinder electrical flow and product performance during defibrillation.
- RECALL
There exists a possibility that the Pain Management Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).
- RECALL
The integrity of the sterile unit package may become compromised.
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