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ISO 17025 Calibration Accreditation

The certificate attests that Sistagrosa S.A. in Guayaquil, Ecuador fulfills the requirements of ISO/IEC 17025:2017 for calibration. The scope of accreditation includes the calibration of medical devices such as defibrillators, electrosurgical units, infusion pumps, blood pressure devices, ventilators, incubators, and fetal dopplers across various parameters including energy, power, flow, pressure, temperature, and time/frequency. The certificate is valid until October 2022.

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0% found this document useful (0 votes)
75 views4 pages

ISO 17025 Calibration Accreditation

The certificate attests that Sistagrosa S.A. in Guayaquil, Ecuador fulfills the requirements of ISO/IEC 17025:2017 for calibration. The scope of accreditation includes the calibration of medical devices such as defibrillators, electrosurgical units, infusion pumps, blood pressure devices, ventilators, incubators, and fetal dopplers across various parameters including energy, power, flow, pressure, temperature, and time/frequency. The certificate is valid until October 2022.

Uploaded by

ebyjoy
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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You are on page 1/ 4

CERTIFICATE OF ACCREDITATION

The ANSI National Accreditation Board


Hereby attests that

Sistagrosa S.A.
Cdla Guayaquil, Av. Victor H. Sicuret P. Mz11,
S4; Entre Emilio Soro Lenti y Enma E. Ortiz Bermeo
Guayaquil, Ecuador
Fulfills the requirements of

ISO/IEC 17025:2017
In the field of

CALIBRATION
This certificate is valid only when accompanied by a current scope of accreditation document.
The current scope of accreditation can be verified at www.anab.org.

______________________________
R. Douglas Leonard Jr., VP, PILR SBU
Expiry Date: 02 October 2022
Certificate Number: AC-2622

This laboratory is accredited in accordance with the recognized International Standard ISO/IEC 17025:2017.
This accreditation demonstrates technical competence for a defined scope and the operation of a laboratory
quality management system (refer to joint ISO-ILAC-IAF Communiqué dated April 2017).
SCOPE OF ACCREDITATION TO ISO/IEC 17025:2017

SISTAGROSA S.A.
Cdla Guayaquil, Av. Victor H. Sicuret P. Mz11, S4; Entre Emilio Soro
Lenti y Enma E. Ortiz Bermeo
Guayaquil, Ecuador
Víctor Ernesto Pineda Gonzalez Phone: (011) 59 34 2 269 2375
[email protected] www.sistagrosa.com

CALIBRATION
Valid to: October 2, 2022 Certificate Number: AC-2622

Electrical – DC/Low Frequency


Reference Standard,
Expanded Uncertainty of
Parameter/Equipment Range Method, and/or
Measurement (+/-)
Equipment
Defibrillator/AED Tester,
Energy Monophasic
(15 to 360) J (0.013X+ 0.31) J External Pacer Analyzer
/Defibrillator1
Fluke Impulse 7000DP
Defibrillator/AED Tester,
Energy Biphasic
(15 to 175) J (0.018X + 0.4) J External Pacer Analyzer
/Defibrillator1
Fluke Impulse 7000DP
(5 to 300) W
at 200 Ω (0.053X + 1.2) W
Electrosurgery Analyzer
Power/ Electrosurgical 1
at 300 Ω (0.053X + 1.1) W
Fluke QA ES II
at 400 Ω (0.053X + 1.3) W
at 500 Ω (0.053X + 1.3) W

Mass and Mass Related


Reference Standard,
Expanded Uncertainty of
Parameter/Equipment Range Method, and/or
Measurement (+/-)
Equipment
Infusion Pump Analyzer
Flow/Infusion Pump1 (16 to 200) ml/h (0.009 1X + 1.6) ml/h
IDA 4 Plus
Digital pressure gauge
ADDITEL ADT681-02-
Pressure/
(0 to 300) mmHg (0.002 2X + 0.65) mmHg GP5-PSI-N, Vital Signs
blood pressure cuff1
Patient Simulator Fluke
PROSIM 8

Version 003 Issued: August 25, 2020 www.anab.org

Page 1 of 3
Mass and Mass Related
Reference Standard,
Expanded Uncertainty of
Parameter/Equipment Range Method, and/or
Measurement (+/-)
Equipment
Non-Invasive Blood Pressure Vital Signs Patient
/Multi-parameter Monitor (30 to 150) mmHg (0.007 4X + 0.5) mmHg Simulator
(Electrical Simulation)1 Fluke PROSIM 8
Invasive Blood Pressure / Vital Signs Patient
Multi-parameter Monitor (0 to 120) mmHg (0.011X + 1.2) mmHg Simulator
(Electrical Simulation)1 Fluke PROSIM 8
Airway Pressure/Pulmonary
Fluke VT900 Gas Flow
Ventilator-Anesthesia (-100 to 100) cmH2O (0.006 3X + 0.083) cmH2O
Analyzer
Machines1
Airway Flow/Pulmonary
Fluke VT900 Gas Flow
Ventilator- Anesthesia (0.5 to 100) l/min (0.02X + 0.008) l/min
Analyzer
Machines1

Thermodynamic
Reference Standard,
Expanded Uncertainty of
Parameter/Equipment Range Method, and/or
Measurement (+/-)
Equipment
Temperature/ Incubator Analyzer
(25 to 40) ºC 0.77 ºC
Infant Incubator1 Fluke INCU

Time and Frequency


Reference Standard,
Expanded Uncertainty of
Parameter/Equipment Range Method, and/or
Measurement (+/-)
Equipment
Cardiac Rate ECG/Multi- Vital Signs Patient
parameter Monitor (40 to 300) BPM (0.011X + 0.022) BPM Simulator
(Electrical Simulation)1 Fluke PROSIM 8
Cardiac Rate/Fetal Doppler Fetal Simulator
(90 to 180) BPM (0.008 9X + 0.6) BPM
(Electrical Simulation)1 Fluke PS 320
Respiration Rate-Multi- Vital Signs Patient
Parameter Monitor (20 to 60) BrPM (0.06X + 0.033) BrPM Simulator
(Electrical Simulation)1 Fluke PROSIM 8
Digital Caliper/
Cardiac Rate/
Vital Signs Patient
Electrocardiogram (Electrical (40 to 300) BPM (0.016X – 0.034) BPM
Simulator Fluke
Simulation)1
PROSIM 8

Version 003 Issued: August 25, 2020 www.anab.org

Page 2 of 3
Calibration and Measurement Capability (CMC) is expressed in terms of the measurement parameter, measurement range, expanded uncertainty of measurement and
reference standard, method, and/or equipment. The expanded uncertainty of measurement is expressed as the standard uncertainty of the measurement multiplied by a
coverage factor of 2 (k=2), corresponding to a confidence level of approximately 95%.
Notes:
1. On-site calibration service is available for this parameter, since on-site conditions are typically more variable than those in the laboratory, larger measurement
uncertainties are expected on-site than what is reported on the accredited scope.
2. X = reading of the unit under test.
3. This scope is formatted as part of a single document including Certificate of Accreditation No. AC-2622.

Version 003 Issued: August 25, 2020 www.anab.org

Page 3 of 3

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