Example: barber
PREVENA PLUS - Acelity
Conforms to: IEC 60601-1, IEC 60601-1-6, IEC 60601-1-11, IEC 60601-1-8 Electrical Equipment Interference Cell phones or other similar products could affect the therapy unit. Move the therapy unit away from these devices if interference is suspected. Use patch strips or excess drape to seal leak. Press firmly around dressing edges. Charging ...
Tags:
Information
Domain:
Source:
Link to this page:
Documents from same domain
PREVENA INCISION MANAGEMENT SYSTEM - Acelity
www.acelity.comMANAGEMENT SYSTEM PREVENA ... if frank blood is seen in the tubing or in the canister, the patient should leave the PREVENA™ Dressing in place, turn off the therapy unit and seek immediate emergency medical ... Hyperbaric Oxygen Therapy (HBO): Do not take therapy units or PREVENA™ Dressings into a hyperbaric oxygen chamber.
CLINICAL GUIDELINES
www.acelity.comV.A.C.® Therapy and Hyperbaric Oxygen ... be readily integrated into the clinician’s wound healing practice, to help optimize patient care. This advanced wound healing technology is coupled with microprocessor-controlled therapy ... • Ensure a …
CLINICAL GUIDELINES
www.acelity.comV.A.C.® Therapy and Hyperbaric Oxygen ... be readily integrated into the clinician’s wound healing practice, to help optimize patient care. This advanced wound healing technology is coupled with microprocessor-controlled therapy ... • Ensure a …
PREVENA PLUS 125 THERAPY UNIT WITH PREVENA PLUS …
www.acelity.com125 and PREVENA PLUS ™125 Therapy Units are intended to aid in reducing the incidence of seroma; and in patients at high risk for post-operative infections, aid in reducing the incidence of superficial surgical site infection in Class I and Class II wounds. • The device is not intended to treat surgical site infection or seroma.
PREVENA 125 THERAPY UNIT WITH PREVENA 45ML …
www.acelity.comreducing the incidence of seroma; and in patients at high risk for post-operative infections, aid in reducing the incidence of superficial surgical site infection in Class I and Class II wounds. • The device is not intended to treat surgical site infection or seroma.
Related documents
List of recognised standards - Japan - IMDRF
imdrf.orgMedical electrical equipment_- Part_1: General requirements for basic safety and essential performance_- Interpretation sheet_2 : IEC 60601-1-1 . 2000-12: N . Medical electrical equipment_- Part_1-1: General requirements for safety; Collateral standard: Safety requirements for medical electrical systems : Y. N
BLOOD PRESSURE UNIT USER’S MANUAL
www.medline.comEN 60601-1 Safety requirements for medical electrical equipment EN 60601-1-2 Electromagnetic compatibility and safety for medical electrical equipment EN 14971 Risk analysis for medical devices in accord with requirement in section 21 of CMDR'S
ISO 26262: Functional Safety Standard for Modern ... - Rohm
fscdn.rohm.com60335-1 (Household and Similar Electrical Appliances), IEC 61513 (Nuclear Power Plants), IEC 62278 (Railway Applications), ISO 13482 (Robots and Robotic Devices), IEC 60601 (Medical Electrical Equipment), EN 81 (Elevators), EN 50156-1 (Electrical Equipment for Furnaces).
FREE download 60601-1.com/download
60601-1.comThis checklist covers the IEC 60601-1, Edition 3.1 requirements for the labeling and the accompanying documents (IFU) of Medical Electrical Equipment. It also includes information and interpretations for the clause requirements, as applicable.
Medical Device Regulations and Utilization of ...
www.mhlw.go.jpClause 1 Medical devices should be designed and ... JIS Z 4751-2-54:2012 is based on IEC 60601-2-54:2009 (MOD) 14 Example of Certification Standard Essential Principles Checklist. ... ISO/TC 194 Biological and clinical evaluation of medical devices IEC/TC 62 Electrical equipment in medical practice ISO/TC 215 Health informatics
Welch Allyn® Spot™ Vision Screener Model VS100 - Hillrom
www.welchallyn.comconnectors are intended for connection of only other medical devices, medical systems or non-medical devices complying with IEC 60601-1, or other IEC standards appropriate to the device. For example, a printer connected via USB must comply with IEC 60950. Connecting additional unapproved devices to the device might increase chassis or subject