SchureMed 800-0342-R Great White Robotic Stirrups Instructions
- June 11, 2024
- SchureMed
Table of Contents
800-0342-R Great White Robotic
Stirrups Instructions
800-0342-R Great White Robotic Stirrups
Instructions for Use
Great White Robotic Stirrups 800-0342-R
Great White Robotic Stirrups with Fins 800-0342-RF
Replacement Pads
Premium Stirrup Boot Pads, Set 508-1354
Platinum Stirrup Boot Pads, Set 508-1415
INTENDED USE
Great White Robotic Stirrups are a patient positioning accessory used in
Gynecology, Urology, and laparoscopic procedures. They provide a safe system
for positioning the legs up to 600 lb. (272 kg) patients in a variety of
lithotomy/abduction positions. The intended users of this device are medical
professionals within hospitals and surgery centers.
GENERAL SPECIFICATIONS
Device Dimensions (maximum)
- Height: 35.25” +/- 0.5” (90 cm +/- 1 cm)
- Width: 9” +/- 0.5” (23 cm +/- 1 cm)
- Depth: 14” +/- 0.5” (36 cm +/- 1 cm)
- Device Weight Per Stirrup: 10 +/- 0.5 lbs. (4.5 +/- .22 kg) (with pad)
- Range of Motion: 60° to -55° lithotomy range, -9° to 25° adduction to abduction
- Single-person installation
- Connects to seat section of surgical table
- Store stirrups on transport/storage dolly (P/N 800-0074R sold separately)
GENERAL INFORMATION
- Product not made with Natural Rubber Latex
- Device supports 600 lb. (272 kg) proportional patient load (6’4″ (193 cm) tall patient per 99% human body model)
- Product warranty covers product from manufacturing defects for period of 2 years
- CE marked medical device according to MDR (EU) 2017/745
- Life of device is 5 years under normal use
- Store device between -4°F to +86°F (-20°C to 30°C)
INSTRUCTIONS
Become familiar with patient positioning device’s features before use with patient. Always practice on a nurse, physician or appropriate volunteer prior to using clinically.
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Attach Springboks Clamps P/N 800-0338 on accessory rails in same location on opposite sides of surgical table at patient’s hip joints.
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Prior to placing device into Spring Loc Clamp, identify patient’s left and right side stirrup indicated on boot label.
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Insert stirrup blades into clamps. Tighten clamps by turning handle to the right.
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Ensure patient is positioned on surgical table in accordance with procedure and surgeon requirements.
WARNING!! To prevent patient or operator injury from inadvertent stirrup movement, securely tighten accessory clamp and boot clamp.
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Support patient’s leg by grasping heel in one hand and underside of knee with other hand. Gently flex knees and transfer leg into boot, then secure boot straps.
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To achieve appropriate leg/foot position, loosen boot clamp. Adjust boot to desired position and re-tighten clamp. Ensure patient’s heels are securely seated in boot heels.
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To achieve appropriate lithotomy and abduction positions, squeeze trigger, adjust to desired position and release to lock.
Note: Free-floating boot is designed to rotate about pivot shown above through-out the full range of motion, reducing risk of superficial nerve injury.
TAKE DOWN
- Loosen clamps and remove stirrups by lifting them out of clamps
- Remove accessory clamps from side rails
COMPONENT OVERVIEW
Great White Robotic Stirrups and Great White Robotic Stirrups with Fins
provide a safe system for positioning the legs up to 600 lb. (272 kg) patients
in a variety of lithotomy/abduction positions.
Other required products for use:
800-0338 Spring Loc Clamp
800-0338-EU Spring Loc Clamp
800-0338-JPN Spring Loc Clamp
800-0338-SWISS Spring Loc Clamp
Replacement Pads
508-1354 Premium Stirrup Boot Pads, Set
508-1415 Platinum Stirrup Boot Pads, Set
DISPOSAL
- General – Prevent infection by cleaning and disinfecting product before disposal
- Packaging – Dispose packaging material via household waste according to national requirements
- Shure Med accepts back used or retired products – or dispose of product in accordance with national requirements
PRODUCT USE WARNINGS
WARNING! Maximum load should not exceed appropriate proportion of a
patient weighing 600 lbs. (272 kg). Use care with low-maximum load capacity
surgical tables that accessory rails are not overloaded.
WARNING! Hazards result from incorrect use. Strictly follow instructions
for use with your Operating Table system.
WARNING! Surgical table load capacities may be less. Never overload a
surgical table. Device is intended for mounting on side of a rail of a
surgical table only.
WARNING! Do not reuse device if there are obvious signs of damage or
functional issues. Consult manufacturer before reusing.
CLEANING RECOMMENDATION
Follow current Association of perioperative Registered Nurses Journal
Guidelines for proper cleaning and disinfection procedure.
WARNING!
Adhere to standards for blood-borne pathogens from the Occupational Safety and
Health Administration.
Use recommended protective clothing, gloves, masks and eye protection to clean
accessory.
CAUTION
Strictly read/follow manufacturer’s directions for cleaning fluids. DO NOT use
cleaners containing phenolics.
- Remove major contaminants from accessory with disposable materials. Follow appropriate bio-hazard waste disposal procedures.
- Apply cleaning fluid liberally to entire accessory and wipe with clean, lint-free cloth until all moisture and cleaning fluid is removed from accessory
- Let accessory dry
USER NOTICE
Any serious incident that has occurred in relation to the device should be
reported to the manufacturer and the competent authority of the Member State
in which the user and/or patient is established.
Basic UDI-DI: 081001460F0040DU
Symbol Glossary
Symbol
| Title| Symbol Description
---|---|---
| Manufacturer| Indicates the medical device manufacturer.
| Authorized Representative in the European Community| Indicates the
authorized representative in the European community.
| Use-by Date| Indicates the date after which the medical device is not to be
used.
| Batch Code| Indicates the manufacturer’s batch code so that the batch or lot
can be identified.
| Catalogue or Item Number| Indicates the manufacturer’s catalogue or item
number so that the medical device can be identified.
| Serial Number| Indicates the manufacturer’s serial number so that a specific
medical device can be identified.
| Caution| To indicate that caution is necessary when operating the device or
control close to where the symbol is placed, or to indicate that the current
situation needs operator awareness or operator action in order to avoid
undesirable consequences.
| Medical Device| Indicates the item is a medical device.
| Unique Device Identifier| Indicates a barcode as containing unique device
identifier information.
| CE Marking| European Conformity.
| Patient Use| Indicates the item is a single patient use medical device.
Manufacturer
Schemed (081001460) Authorized Representative
Emergo Europe, Prinsessegracht 20, 2514 AP The Hague, The Netherlands