BLAddERSCAN BVI 3000
CERTIFICATE OF CALIBRATION & COMPLIANCE
Instrument SN:
Probe SN:
Asset Number:
Location:
The tests performed by the technician on the equipment listed above confirmed that it met all applicable product
manufacturing and test specifications. Certification service is performed in compliance with Verathon Inc.
manufacturing test specifications and equipment.
Verathon recommends that certification of calibration be performed once a year.
Today’s Date: Next Certification Date:
COMPLIANCE WITH “CERTIFY THE SYSTEM” PROCEdURE
Check the cosmetic appearance
Check power and backlight functions
Console settings and software are correct
System passes self‑test
System passes print‑test
Calibration date is correct
System passes string‑test
Scan results are accurate (record in table below)
Battery charger functions properly
Replaced batteries? Yes No
SCAN RESULTS ON TISSUE‑EQUIVALENT PHANTOM
Ensure that you capture at least one scan result in each scan mode. If desired, collect three scan results in each mode
to ensure consistency. Confirm the results are within the accuracy range of the phantom’s certified value.
Certified volume for phantom: mL
SCAN MODE SCAN #1 SCAN #2 SCAN #3 WITHIN RANGE?
Male mode Yes No
Female mode Yes No
Comments:
CERTIFIEd ON BEHALF OF VERATHON INC. BY:
Technician’s Signature Date
Global Headquarters
Verathon, Inc.
20001 North Creek Parkway
Bothell, WA 98011 U.S.A.
Tel: 425.867.1348 / 800.331.2313 (US & Canada)
Fax: 425.883.2896
Verathon Medical Australia
Unit 9, 39 Herbert Street
St Leonards NSW 2065
Tel: +61 2 9431 2000 / 1800 613 603 (Australia)
Fax: +61 2 9475 1201 / 1800 657 970 (Australia)
European Headquarters
Verathon Medical Europe B.V.
Willem Fenengastraat 13
1096 BL Amsterdam
The Netherlands
Tel: +31 (0) 20 210 30 91
Fax: +31 (0) 20 210 30 92
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