3B Medical Lumin LM3000 Talimatlar Kılavuzu - Sayfa 2
Aksesuarlar 3B Medical Lumin LM3000 için çevrimiçi göz atın veya pdf Talimatlar Kılavuzu indirin. 3B Medical Lumin LM3000 14 sayfaları. Instructions for healthcare facilities: bioburden reduction uv system user's manual
Ayrıca 3B Medical Lumin LM3000 için: Kullanıcı Kılavuzu (7 sayfalar)
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LUMIN LM3000 BIOBURDEN REDUCTION UV SYSTEM
The U.S. Food and Drug Administration has issued an Emergency Use Authorization (EUA) for the emergency
use of the Lumin LM3000 Bioburden Reduction UV System (hereafter referred to as the "Lumin LM3000") for
use in bioburden reduction of 3M model 1860 N95 respirators (also referred to as "compatible N95
respirators") for single-user reuse by healthcare personnel (HCP) to supplement the Centers for Disease Control
and Prevention (CDC) reuse recommendations. Healthcare personnel should follow these instructions, as well
as procedures at their healthcare facility, to prepare compatible N95 respirators for bioburden reduction using
the Lumin LM3000.
The Lumin LM3000 has been authorized by FDA under an EUA for bioburden reduction of 3M model 1860 N95
respirators only for single-user reuse by HCP to supplement CDC reuse recommendations to prevent exposure
to SARS-CoV-2 and other pathogenic biological airborne particulates. The Lumin LM3000 has not been FDA
cleared or approved for this use. The Lumin LM3000 is authorized only for the duration of the declaration that
circumstances exist justifying the authorization of the emergency use of medical devices, during the COVID-19
outbreak, under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1),
unless the authorization is terminated or revoked sooner.
Respirators that are NIOSH-approved before bioburden reduction (https://wwwn.cdc.gov/niosh-cel/) only
retain their NIOSH approval status post-bioburden reduction if the respirator manufacturer permits the use of
the bioburden reduction method with the specific system and cycle parameters. To determine the NIOSH
approval status of a specific bioburden-reduced NIOSH-approved respirator, please check with the respirator
manufacturer and/or the respirator labeling. If a respirator is no longer NIOSH-approved after use of the
particular bioburden reduction method, its performance (i.e., fit, filtration, and breathability) might not
consistently meet NIOSH-approved N95 standards.
Equipment protected throughout by double insulation or reinforced insulation.
Refer to instruction manual.
Important information concerning your safety or the operation of your device.
The Lumin LM3000 is only authorized for use with the 3M model 1860 N95 respirators. The Lumin LM3000 is not
authorized for use with any other respirator model or other types of personal protective equipment.
The Lumin LM3000 Bioburden Reduction System is intended for bioburden reduction of compatible N95
respirators for single-user reuse by healthcare personnel serving in healthcare settings, including
nursing homes, assisted living facilities, primary care offices, and clinics, to supplement CDC reuse
recommendations.
EXPLANATION OF SYMBOLS USED
COMPATIBLE N95 RESPIRATORS
INTENDED ENVIRONMENTS FOR USE
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