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Tag: medical
Murata Achieves IEC 60601 MOOP 3rd Edition Medical Safety Certification for 2 x4 120W Power ...
2014-02-15 06:00:00| Industrial Newsroom - All News for Today
MVAB120 Series<br /> <br /> Murata announced today that its MVAB120 series of single output 120 Watt AC-DC power supplies now complies with the third edition of the EN/UL/IEC60601 and ANSI/AAMI ES60601-1 third edition MOOP (means of operator protection) medical safety standard. With this certification, the MVAB120 series can now be used for any non-patient-contact medical application in addition to being suitable for use in networking, industrial automation, and test/measurement equipment as ...This story is related to the following:Health, Medical and Dental Supplies and EquipmentSearch for suppliers of: Open Frame Power Supplies |
Tags: power
edition
medical
safety
Discovery of Mass Graves Halts Mississippi Medical Center Project
2014-02-14 20:20:47| ENR.com: Headline News
The property was once the site of the former Mississippi State Insane Asylum and a potters field.
Tags: center
project
medical
mass
Medical Air Connector enhances filling applications.
2014-02-13 14:30:59| Industrial Newsroom - All News for Today
Available with brass or aluminum body featuring brass wetted components, MediMate CGA 950 offers one-hand connection and seamlessly integrates with any existing 950 system. Product does not require any twists or turns to fill compressed gas cylinders; operators can, within seconds, connect to CGA 950 valve and lock into place with forward movement of actuator lever. Along with straight-flow, 180° termination port, feaures include FDA-grade Viton® elastomer seals and 3,600 psi rating. This story is related to the following:Health, Medical and Dental Supplies and EquipmentSearch for suppliers of: Medical Connectors
Tags: air
medical
applications
filling
Polymicro Technologiesa Achieves U.S. Fda QSR Medical Device Registration
2014-02-13 12:41:02| Electronics - Topix.net
Polymicro Technologies , a subsidiary of Molex Incorporated , announced its recent registration and compliance with the U.S. Food and Drug Administration 21 CFR 820 Quality System Regulation .
Tags: medical
registration
device
fda
FDA to Require Electronic Filing for Medical Device Reporting
2014-02-13 09:00:00| Expeditors Newsflash - Americas Edition
Expeditors Newsflash - Americas Edition
Tags: medical
require
electronic
device
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