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Sterilizacija

Avoid Long Delays in Instrument Decontamination, Reprocessing

Leaving instruments unprocessed for any period of time can lead to the development of biofilm. The recommendation is to begin the cleaning process as soon as possible. As a matter of fact, a number of manufacturer’s instructions for use (IFUs) are now specifying the time frame that cleaning should be implemented. This ranges from “immediately after use” to “within 10, 20 ali 30 minut;” it varies with the device/instrument manufacturer. The manufacturer’s IFUs should always be followed.

APP: Point #73

Kot predsednik Združenja poklicnih Piercers, Imam redno uredniško stolpec v reviji Point. Izdaja 73 editorial Please enjoy

APP konferenca kmalu!

  KONFERENCA je skoraj na nas! KONFERENCA ADVANCED (ONLINE) REGISTRACIJA bo ugasnil opolnoči MAJA 17, PST koli spremeniti registracijo bi bilo treba …

Zaslužiti a STATIM 2000 G4

FDA navodila o sterilizatorji

Kaj avtoklavi so za sterilizacijo votla odobrila FDA?
Standardi za avtoklavi, ki lahko obdela elemente z lumnov so javno dostopni preko spletne strani FDA.

Effects of Non-Condensable Gases (NCGs) on Steam Sterilisation Processes

A study conducted by Prof. von Eiff of University of Münster in hospitals in North Rhine Westphalia and Lower Saxony revealed that, in particular, 40% of hollow instruments released for use were not sterile (4). One reason for such problems is that the classic biological and/or well-integrated chemical indicators can attest to the sterility of supplies only at those locations at which they are positioned. But in general these indicators cannot be placed at those sites within the instrument which are most difficult to access, hence the established practice of using such indicators is not suitable for providing insights into the sterility of lumened devices.

Brave

Welcome to Bravo! A fractionated vacuum autoclave from SciCan Buy a Bravo now BRAVO chamber autoclave Features Fractionated vacuum

Enkratno zaviti

Lahko neuporabljene zaviti artikli se sterilizirati, ponovna uporaba izvirnega obloge?

Vračajo izsečki bolnikom

Pri razvijanju politike o ponovni termoterapija bolnikov [ali prej obrabljeni telesa nakit strankam] Obstaja veliko skrbi in vprašanj, ki jih je treba upoštevati in obravnavati.

Sharpies za označevanje

“Večina Sharpies validirani ne, za industrijsko uporabo ali za uporabo v pogojih sterilizacija. Obstaja nekaj Sharpie označevalcev, ki v skladu z ASTM standardne D4236, kar pomeni, da izdelek je ocenil toksikolog za akutne in kronične toksičnosti in varnostni list (SDS) identificira sestavine kot nevarni vse kronične zdravstvene, skupaj z navodili za varno uporabo. Peresa, ki nosijo pečat AP z notacijo “v skladu z ASTM D4236″ (glej desno) so označevalci, ki se lahko uporabljajo za označevanje vaših paketov.”

OPTIM 33TB protokol

Protokol za prehod na OPTIM 33 TB enostopenjski čistejše razkužilom, in hitrega referenčnega priročnika za uporabo tatoo in Piercing