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SKID-E, PRO SKID-E, PRO SKID-E MAX,
SKID-E READY, SKID-OK, SKID-OK MAX
Caution: U.S. Federal law restricts this device to sale by or on the order of a licensed healthcare practitioner
This appliance conforms with the Directive 93/42/CEE "Medical Devices"
Guarantee of Quality system for the production and the final control of the products certified by
the notifying body TÜV SÜD Product Service GmbH.
General information
Warnings
Product description
User's Manual
Evacuation chairs
INDEX
page 2
page 3
page 5
1
Operating instructions
Maintenance and cleaning
Accessories and spare parts
page 7
page 11
page 12
First edition: 06/12/10
Rev. 4: 09/02/17
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Table of Contents
Related Manuals for Spencer PRO SKID-E
Summary of Contents for Spencer PRO SKID-E
- Page 1 User’s Manual SKID-E, PRO SKID-E, PRO SKID-E MAX, SKID-E READY, SKID-OK, SKID-OK MAX Evacuation chairs Caution: U.S. Federal law restricts this device to sale by or on the order of a licensed healthcare practitioner This appliance conforms with the Directive 93/42/CEE “Medical Devices”...
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Page 2: General Information
Customer Care Service on tel. 0039 0521 541111, fax 0039 0521 541222, e-mail info@spencer.it or write to Spencer Italia S.r.l. - Strada Cavi, 7 - 43044 Collecchio (Parma) - ITALY. In order to facilitate the assistance service, please always indicate or communicate the serial number (SN) shown on the label applied on the box or on the device. -
Page 3: General Warnings
This register which will certify the eligibility of the operators to use the Spencer device has to be kept for a period of 10 years after the disposal of the device itself. This register will be made available to the Competent Authorities and/or Manufacturer if requested. -
Page 4: Specific Warnings
This register which will certify the eligibility of the operators to use the Spencer device has to be kept for a period of 10 years after the disposal of the device itself. This register will be made available to the Competent Authorities and/or Manufacturer if requested. -
Page 5: Intended Use
3. PRODUCT DESCRIPTION Intended use The evacuation chairs Spencer SKID-E, PRO SKID-E, PRO SKID-E MAX, SKID-E READY, SKID-OK and SKID-OK MAX are devices for seated patient transport, in cases in which another cumbersome device can not guarantee adequate and safe transport. The use of passive belts that slide on the stairs ensure a high safety level requiring no effort which permits safe and reliable evacuation during emergency operations. - Page 6 Models SK20001E SKID-E Evacuation chair with silver frame and black sheet SK10001E PRO SKID-E Evacuation/transport chair with yellow frame and black sheet SK10201E PRO SKID-E Evacuation/transport chair with silver frame and black sheet SK20101E SKID-E READY Evacuation chair with fixed backrest, yellow frame and black sheet...
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Page 7: Operating Instructions
Reference standards Reference Title of document MDD 93/42/CEE European Directive about Medical Devices Modifications to 90/385/CEE Directive about active implants, Directive 93/42/CEE about medical devices MDD 2007/47/CEE and Directive 98/8/CE about the introduction of biocides onto the market Application of the 93/42/CEE Directive about Medical Legislative Decree 24/02/1997, n. - Page 8 1 - Using both breaks, block both front Ø100 mm wheels turned in inside direction. 2 - Only PRO SKID-E and PRO SKID-E MAX models: Disengage the rear handles (if positioned as in fig. E - F) by inserting the hooks in the blocking system (fig. G).
- Page 9 5 - Attach the belt around the body which will block the seat in position. Fig. E Fig. F Fig. G 4.3.3 Patient transport on stairways - Downstairs 1 - Apply the procedure described in paragraph 4.3.1. 2 - Grab the main handle firmly with both hands and let the patient sit on the chair. Make sure during this operation that both front Ø...
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Page 10: Troubleshooting
4.3.4 Patient transport on stairways - Upstairs (PRO SKID-E and PRO SKID-E MAX MODELS ONLY) This operation is possible with the PRO SKID-E model only. 1 - Apply the procedure described in paragraph 4.3.1. 2 - Secure the patient to the device using the special safety belts for the head and the body. -
Page 11: Maintenance And Cleaning
Please note that you must do the cleaning as described in paragraph 5.1 and verify functionality before and after each use. Spencer Italia S.r.l. declines any responsibility for the proper functioning or damages caused to the patient or user by the use of devices not subject to routine maintenance, warranty and will void the compliance to the Medical Device Directive 93/42/CEE. -
Page 12: Accessories And Spare Parts
Spencer Italia S.r.l. will take no responsibility for the incorrect functioning or any damage caused by a device that has not undergone regular revision. - Page 13 ATTACHMENT A – TRAINING REGISTER The product must be used by trained personnel only, having attended specific training for this device and not for similar products. Keep this document at least 10 years from the end of life of the device. Training method Training date Operator’s...
- Page 14 The information contained in this document could be modified without any warning and is not to be intended as a commitment on behalf of Spencer Italia S.r.l. Spencer products are exported to many countries and the same identical regulations are not always valid. For this reason there could be differences between the description here described and the product actually delivered.
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