This document excludes hazards related to bacteria, moulds, yeasts, viruses, transmissible spongiform encephalopathy tse agents and other pathogens. En 610101 3rd edition compliance required in eu by october. Particular requirements for refrigerating equipment iec 61010 2011. Rdts tb ag mpt64 rapidsd bioline cakramas 62811945609. En 61010 2011 en 61010 2011 safety requirements for electrical equipment for measurement, control, and laboratory use part 2011. W8710prolene 50 teknologi hemoseal non absorbable suture pigmented undyed. Iec 610101 testing en 60601 or iec 60601 is the european harmonized standard to meet the medical device directive. Safety requirements for electrical equipment for measurement, control and laboratory use part 1. Rdtes infeksi malaria alat tes malaria plasmodium spd pf ag cakramas supplier.
This part of iec 61010 applies to equipment intended for in vitro diagnostic ivd medical purposes, including selftest ivd medical purposes. Note 2 this symbol corresponds to that given in iso 70001051 and to symbol number 5. Ophthalmic instrument catalogue storz ophthalmic instruments. This standard is addressed for the last time in the official journal publication of the 20170908. This part of iec 61010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used. Products sold into the eu must comply with the 3rd edition of en 610101 by october 20. Safety requirements for electrical equipment for measurement, control, and laboratory use part 1.
Low voltage lvd directive 201435eu last official journal reference. Ul 610101 safety requirements for electrical equipment for. Bbraun general catalogue sutures by ultradental issuu. The uspnf, whicn is released on november 1 of each year, becomes official on may 1 of the following year. Guide safe testing and measuring staubli electrical connectors. Do not use this device in close proximity to sources of strong electromagnetic radiation e. This sixmonth implementation timing gives users more time to bring their methods and procedures into compliance. No pollution or only dry, nonconductive pollution occurs. En 60601 or iec 60601 is the european harmonized standard to meet the medical device directive. Products sold into the eu must comply with the 3rd edition of en 61010 1 by october 20. It appears with similar meaning in other documents e. Iec 610101, edition 3 white paper pdf analog devices. This part of iec 61010 specifies general safety requirements for the following. Prolene 70 8696g, blue 45cm, 38 circle surgical suture non absorbable suture clear undyed.
Our breadth, established objectivity and proven history mean we are a symbol of trust, enabling us to help provide peace of mind to all. However, chemicals introduce potential hazards and thermo has adopted the following position with regard to the subject of heated surfaces and volatile chemicals used in medical laboratories. Sixmonth implementation guideline the united states pharmacopeianational formulary and its supplements become official six months after being released to the public. En 60601 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems. Read below for en 61010 1 3rd edition compliance required in eu by october 20. En 610101 3rd edition compliance required in eu by. This part of iec 61010 specifies general safety requirements for the. Note 1 synonyms for do not reuse are single use, use only once. En 606011 note this symbol corresponds to or that given is in not isospecified. The shandon tissuewave 2 as supplied, complies with en 61010 1. Read below for en 610101 3rd edition compliance required in eu by october 20. When verifying a clearance within equipment, it is necessary to ensure that the specified voltage appears.
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