UL 1363A OR UL 60601 CODE

This article was first published as a blog post at . UL 1363A: Basic safety standard for power strips integrated as components of a larger system where they supply power to equipment in a movable assembly that is rack, table or pedestal-mounted. Make sure you know the rules in case you need to some surveyor education. There are many credible reports of CMS and Joint Commission surveyors who donРІР‚в„ўt understand the РІР‚Сљpower stripРІР‚Сњ rules. Use good quality power strips that are appropriate for each location and take damaged power strips out of service when they are found during environmental tours (hazard surveillance rounds). CMS and the Joint Commission are silent on this topic. Power strips used outside of Patient Care Rooms. The РІР‚Сљelectrical and mechanical integrity of the assembly must be regularly verified and documented through an ongoing maintenance program.РІР‚Сњ To me, that means visual inspection with simple CMMS documentation. You no longer need to block off unused receptacles on the SPRPT. There are some requirements regarding ampacity (see the AAMI News article for details) that should be pretty easy to meet if youРІР‚в„ўre using genuine SPRPTs. Inspection of SPRPTs used in the Patient Care Vicinity. Power strips used in Patient Care Rooms outside of the Patient Care Vicinity. They must be permanently attached to a rack-, table-, pedestal-, or cart-mounted assembly of patient-care-related electrical equipment. They may not be used to power non-patient-care-related electrical equipment. Power strips for use in the Patient Care Vicinity. It should also include the CMS definitions of Relocatable Power Tap (a power strip labeled as compliant with UL 1363) and Special Purpose Relocatable Power Tap (a power strip labeled as compliant with UL 1363A OR UL 60601-1). The policy should include the NFPA 99 (2012) definition for Patient Care Room, Patient Care Vicinity, and Patient-care-related Electrical Equipment. Here are the key points:Р”Вefine your terms. It includes a policy template and suggests some ideas for writing your own policy. Accrediting organizations, like The Joint Commission, donРІР‚в„ўt help much.Р”Р‡or the November 2017 issue of AAMI News, I wrote a one-page article in an attempt to clear things up.

UL 1363A OR UL 60601 CODE

Learn more about medical device recalls.Р”Сћ Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.Р”Р€ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 Р’В§7.55.Confused about CMS requirements for РІР‚Сљpower strips,РІР‚Сњ some of which are technically referred to as RPTs (relocatable power taps)? YouРІР‚в„ўre not alone! Requirements from CMS (Centers for Medical and Medicaid Services) are not easy to turn into a coherent policy. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. For medical inquiries, the accounts were directed to contact Hospira Medical Communications at 1-80.Р”РЋ A record in this database is created when a firm initiates a correction or removal action. They were also requested to complete the enclosed reply form and return it to Hospira by fax at 1-26, indicating the amount of product placed on hold for return, if they further distributed the product and if they notified their retail customers. If they distributed the affected product further, they were instructed to sub-recall the product from their sub-accounts. The accounts were instructed to examine their inventory for the affected product and quarantine it immediately, and Stericycle at 1-80 to obtain a return kit for returning the affected product. Hospira sent Urgent Device Recall letters dated 7/1/10 to their direct accounts on 7/2/10 via Federal Express 2 day delivery, informing them of the potential for electrical shock, electrical short, or electrical fire, since the power packs were not certified to UL 60601 standard or Subject 1363A of UL standard 1363 for relocatable power taps intended for use with medical equipment. Potential problems could include electrical shock, electrical short or electrical fire. The Power Pack Accessory is not certified to UL 60601 standard or Subject 1363A for relocatable power taps intended for use with medical equipment. Field Drive, Lake Forest, IL 60045 part number 3, Modo #HSP1700, Model Tripp-Lite PS-415-HGР”Р„ccessory power pack used for use with medical devices. Hospira Accessory Power Pack a 4 outlet power strip with a custom pole clamp bracket to attach to the IV pole with the infusion pump Distributed by: Hospira, Inc., 275 N. Class 2 Device Recall Hospira Accessory Power Pack

Ul 1363a or ul 60601