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Minor Procedure Table, Phenolic 800-0026-MI-P
Minor Procedure Table, Carbon Fiber 800-0026-MI-CF
Minor Procedure Table Pad 508-0072
Its function is to provide a stable platform for all arm and hand surgeries. The intended users of this device are medical professionals within hospitals and surgery centers.
INSTRUCTIONS FOR USE
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.
Device Dimensions (maximum)
Attach clamps (sold separately) to side rail and place them approximately 1' (31 cm) apart (as shown)
- Insert mounting rods into clamps (as shown)
- Adjust procedure table so that it is level with surgical table pad. Secure table to accessory rail using the Locking Knobs of the clamps (as shown)
- Includes 1" (3 cm) pressure management pad
- Clamps sold separately
- Patient Weight Capacity: 600 lbs. (272 kg) patient, 20 lbs. (9 kg) @ far end of table, 41 lbs. (18.5 kg) in center of table
- Length: 30” +/- 0.5” (76 cm +/- 1 cm)
- Width: 15” +/- 0.5” (38 cm +/- 1 cm)
- Maximum Raised Height: 3.5" +/- 0.5” (9 cm +/- 1 cm)
- Phenolic Depth: .375" +/- 0.5” (.95 cm +/- 1 cm)
- Phenolic: Device Weight: 10 +/- 0.5 lbs. (4.5 +/- .22 kg)
- Carbon Fiber Depth: .25” +/- 0.5” (.64 cm +/- 1 cm)
- Carbon Fiber: Device Weight: 9 +/ 0.5 lbs. (4 +/- .22 kg)
- Hand Table Mounting Post: 6”L (15 cm)
- Attaches to rail of surgical table at any point on rail
- Single-person installation
Minor Procedure Tables, Phenolic or Carbon Fiber, are surgical table extensions that attach to all rails.
Replacement Pad: 508-0072 Minor Procedure Table Pad
Two Clamps Required: Choose Universal Clamp for US or Deluxe Rail Clamp for Outside US
US – Universal Rail Clamp
Outside US – Deluxe Rail Clamp
- US: 0.374” x 1.122” (9.5 mm x 28.5 mm) PN# 800-0085
- Denyer: 0.236” x 1.496” (6 mm x 38 mm) PN# 800-0248-DEN
- Europe: 0.394” x 0.984” (10 mm x 25 mm ) PN# 800-0248-EU
- Eschmann (UK): 0.236” x 1.260” (6 mm x 32 mm) PN# 800-0248-UK
- Japan: 0.354” x 1.260” (9 mm x 32 mm ) PN# 800-0248-JPN
- Swiss: 0.394” x 1.181” (10 mm x 30 mm ) PN# 800-0248-SWISS
- Product not made with (NRL) 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
- If damaged in shipping, call Customer Service at (888) 724-8763 or (781) 982-7000 to obtain Return Material Authorization (RMA) number. For product warranty issues, contact Customer Service.
- CE marked medical device according to MDR (EU) 2017/745
- Product is maintenance-free, check product condition before next use
- Life of device is 5 years under normal use
- Store device between -4°F to +86°F (-20°C to 30°C)
- General - Prevent infection by cleaning and disinfecting product before disposal
- Packaging - Dispose packaging material via household waste according to national requirements
- SchureMed accepts back used or retired products - or dispose of product in accordance with national requirements
PRODUCT USE WARNINGS
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.
Hazard resulting from incorrect use. Strictly follow Instructions for Use with your Operating Table system.
Do not reuse device if there are obvious signs of damage or functional issues. Consult manufacturer before reusing.
Strictly read/follow manufacturer’s directions for cleaning fluids. DO NOT use cleaners containing phenolics.
Follow current Association of periOperative Registered Nurses (AORN) Journal Guidelines for proper cleaning and disinfection procedures.
Adhere to standards for blood-borne pathogens from the Occupational Safety and Health Administration (OSHA). Use recommended protective clothing, gloves, masks and eye protection to clean accessory.
- 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
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.
IFU-800-0026-MI-P-CF REV 3.04
Basic UDI-DI: Phenolic Model - 081005737F0022KP
Basic UDI-DI: Carbon Fiber Model - 081005737F0023KR
Latest Revision: 2022-01
eIFU Language Versions
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452 Randolph Street, Abington, MA 02351 USA
Toll Free ( 888 ) 724-8763 | Ph (781) 982-7000
Fax (781) 982-7001 | email@example.com
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