pdfjoiner
12. Disposal 12.1 General Unreliable, damaged or worn out equipment should be removed from service and destroyed. Obsolete but functional equipment has potential resale value but carries with it liabilities under the CPA and LDPA. There are companies who can manage such transactions. The DoH has issued guidelines on the resale of medical equipment in MHRA DB2006(05) [3]. Alternatively, equipment can be donated to a charity. The donor has a moral responsibility to ensure that the recipients are given all relevant information about the equipment. Full service history, usage, fault log, replacement parts and decontamination status should be available when equipment is offered for sale or donation. Disposed equipment must be removed from the capital asset register. 12.2 European WEEE Directive The European WEEE Directive enforces the recovery and recycling of certain types of electrical and electronic equipment (EEE) when it is disposed of. The Directive places a requirement on producers and/or final users to recover and recycle the equipment in line with specific rules. Producers of electrical and electronic items are required to register with the Environment Agency, through organisations referred to as ‘compliance schemes’, and are required to provide information relating to material content and recycling [12]. 12.3 Re-use of equipment Equipment that may be used on more than one patient should be decontaminated or sterilised according to manufacturer’s instructions and the AAGBI guidelines (see Infection Control in Anaesthesia 2, 2008) [13]. Some equipment has a limited 25
number of re-uses (e.g. re-usable LMAs) and a record card or similar device must be used to maintain an accurate record of the number of re-uses. Any equipment bearing the mark of a figure 2 with a line crossed through it is for single use only and must not be re-used. 26
- Page 45 and 46: Suspected anaphylactic reactions as
- Page 47 and 48: Suspected anaphylactic reactions as
- Page 49 and 50: Suspected anaphylactic reactions as
- Page 51 and 52: Suspected anaphylactic reactions as
- Page 53 and 54: Suspected anaphylactic reactions as
- Page 55 and 56: Storage of Drugs in Anaesthetic Roo
- Page 57 and 58: Storage of Drugs in Anaesthetic Roo
- Page 59 and 60: This guideline was originally publi
- Page 61 and 62: Anaesthesia 2015 Checketts et al. |
- Page 63 and 64: Anaesthesia 2015 Checketts et al. |
- Page 65 and 66: Anaesthesia 2015 Checketts et al. |
- Page 67 and 68: Anaesthesia 2015 Checketts et al. |
- Page 69 and 70: Anaesthesia 2016, 71, 1503 Correcti
- Page 71 and 72: Membership of the working party Dr
- Page 73 and 74: 1. Summary 1.1 Safety, quality and
- Page 75 and 76: 3. Responsibility of anaesthetists
- Page 77 and 78: 3.4 The Trust - Medical Devices Man
- Page 79 and 80: 4. Standards 4.1 Medical Devices Di
- Page 81 and 82: 5. Responsibility of manufacturers
- Page 83 and 84: 6. Choosing and trialling equipment
- Page 85 and 86: equipment officer is encouraged to
- Page 87 and 88: EU procurement thresholds Threshold
- Page 89 and 90: When negotiating a purchasing agree
- Page 91 and 92: 9. Shared equipment Many types of e
- Page 93 and 94: Third party servicing is another op
- Page 95: 11. Replacement 11.1 Planned equipm
- Page 99 and 100: Where new equipment is purchased th
- Page 101 and 102: 14. Incident reporting and investig
- Page 103 and 104: available from www.hse.gov.uk 14.4
- Page 105 and 106: DB DoH EBME EC EU FRCA HN HSE IEC I
- Page 107 and 108: 8. OPSI. Statutory Instrument 2006
- Page 109 and 110: Eire Tel: 00353 1 676 4971 Website:
- Page 111 and 112: Peri-operative management of the ob
- Page 113 and 114: Guidelines Peri-operative managemen
- Page 115 and 116: Recommendations 1 Every hospital sh
- Page 117 and 118: 35 30 25 Prevalance (%) 20 15 10 5
- Page 119 and 120: is an increased incidence of prolon
- Page 121 and 122: Figure 2 Relationship between total
- Page 123 and 124: techniques, and when used with neur
- Page 125 and 126: Table 5 The STOP-BANG screening que
- Page 127 and 128: Intra-operative care Preparation of
- Page 129 and 130: Figure 3 Ramping position for obese
- Page 131 and 132: eturn of airway reflexes with desfl
- Page 133 and 134: Table 6 Dosing schedule for thrombo
- Page 135 and 136: A review and meta-analysis by the S
- Page 137 and 138: numbers of staff are needed to roll
- Page 139 and 140: Table 7 Equipment for managing obes
- Page 141 and 142: 11. Schneider HJ, Glaesmer H, Klots
- Page 143 and 144: 44. Edholm D, Kullberg J, Haenni A,
- Page 145 and 146: 75. McKay RE, Malhotra A, Cakmakkay
12. Disposal<br />
12.1 General<br />
Unreliable, damaged or worn out equipment should be<br />
removed from service and destroyed. Obsolete but functional<br />
equipment has potential resale value but carries with it liabilities<br />
under the CPA and LDPA. There are companies who can<br />
manage such transactions. The DoH has issued guidelines on<br />
the resale of medical equipment in MHRA DB2006(05) [3].<br />
Alternatively, equipment can be donated to a charity. The donor<br />
has a moral responsibility to ensure that the recipients are given<br />
all relevant information about the equipment.<br />
Full service history, usage, fault log, replacement parts and<br />
decontamination status should be available when equipment is<br />
offered for sale or donation.<br />
Disposed equipment must be removed from the capital asset<br />
register.<br />
12.2 European WEEE Directive<br />
The European WEEE Directive enforces the recovery and<br />
recycling of certain types of electrical and electronic equipment<br />
(EEE) when it is disposed of. The Directive places a requirement<br />
on producers and/or final users to recover and recycle the<br />
equipment in line with specific rules. Producers of electrical and<br />
electronic items are required to register with the Environment<br />
Agency, through organisations referred to as ‘compliance<br />
schemes’, and are required to provide information relating to<br />
material content and recycling [12].<br />
12.3 Re-use of equipment<br />
Equipment that may be used on more than one patient should<br />
be decontaminated or sterilised according to manufacturer’s<br />
instructions and the AAGBI guidelines (see Infection Control<br />
in Anaesthesia 2, 2008) [13]. Some equipment has a limited<br />
25