Does preventive maintenance have any positive effect on smart transmitters?

V

VALENTINEO

#1
Does preventive maintenance have any positive effect on smart transmitters? or should they be run to failure and replaced?
 
Elsmar Forum Sponsor

Jerry Eldred

Forum Moderator
Super Moderator
#2
I have heard both sides of this issue. This is, again, an issue where you need to evaluate the transmitters performance against the process or application tolerances. If the unit will drift out of an acceptable tolerance limit and still be operating properly (other than the tolerance drift), then there is certainly value, as you need to be sure that the readings it gives you are accurate enough for your need. There are applications, also, where transmitter accuracy is not important, and an inaccurate reading is not important to the correct performance of the process being monitored. Those questions will need to be answered before making such a decision.

The other issue is unstable operation. I certainly won't be the one to give someone an excuse to save moneyt by not doing correct maintenance. It could well be (in some applications) that accuracy is not an issue, but unstable operation is still important. In those cases, maintenance is still important, but for other reasons. I don't believe there is a single correct answer to this. Each application needs to be evaluated to determine how much change in the transmitter's readings and feedback is acceptable. The implications of an incorrect reading from the transmitter must be evaluated, and determination made as to what amount of error can be tolerated. How often, and what type of maintenance is performed must be based on the answer to that evaluation.

------------------
 
Thread starter Similar threads Forum Replies Date
S Does overdue preventive maintenance require an evaluation on product quality? ISO 13485:2016 - Medical Device Quality Management Systems 5
H Preventive Maintenance - Does anyone have a sample of a PM procedure? Document Control Systems, Procedures, Forms and Templates 5
R Does FDA require monitoring competitor device failures for preventive action? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
Hershal Definition Preventive Action - Definition - How does YOUR organization define PA? Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 6
W Preventive 5S - Does anybody have any idea about Preventive 5S? Preventive Action and Continuous Improvement 1
L Does anyone have a Preventive Action Template Document Control Systems, Procedures, Forms and Templates 5
S Does anyone have examples of a Corrective and Preventive action log? Nonconformance and Corrective Action 12
Raffy Preventive Action - Does generating an FMEA help future containment? Preventive Action and Continuous Improvement 2
K Defining Preventive Action - What is it? How does it relate to Continuous Improvement Nonconformance and Corrective Action 18
D Does anyone have a Preventive Action form that I could look at? Document Control Systems, Procedures, Forms and Templates 9
C GTIN & GS1 - what does the law say ? CE Marking (Conformité Européene) / CB Scheme 5
R Does anyone know how ASQ exam requirements are verified? Professional Certifications and Degrees 3
P Does cybersecurity apply to my product? EU Medical Device Regulations 5
Q Does a gage used for a visual verification need to be calibrated? Manufacturing and Related Processes 7
M Does any one know if company is allowed to submit appeal for rejected registration file Other Medical Device Related Standards 0
B Does TUS require load thermocouples? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
B Does anyone copyright their internal QMS documents? Document Control Systems, Procedures, Forms and Templates 24
D MDR technical file: does it need to contain duplicates of controlled documents EU Medical Device Regulations 2
D Does the MDR article 10 (14) needs to be documented word for word in a Procedure? EU Medical Device Regulations 1
S Why does GAGEpack drop the temperature and humidity readings out of the verification event card? Quality Assurance and Compliance Software Tools and Solutions 0
C Determining an as received OOT condition during calibration does not affect measurements taken prior to calibration. General Measurement Device and Calibration Topics 16
D Does the DoC require a technical documentation version? ISO 13485:2016 - Medical Device Quality Management Systems 1
S Local (country) registration of medical devices - Who does it in best case? Other Medical Device Regulations World-Wide 2
G When does containment event not require 100% sort? Nonconformance and Corrective Action 5
H Does this clause mean i must be in compliance with AS9100 or is 9001 enough? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
H Does ISO state in anyway that we MUST keep physical first piece parts? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
XRAY_3121 Class II heating pad - does the power supply have to have IEC 60601-1 testing?? US Medical Device Regulations 5
F Change in address for critical supplier - does NB need to be informed? CE Marking (Conformité Européene) / CB Scheme 20
S Brexit ISO 13485:2016 + Corrigendum - What does a UKCA DoC require? EU Medical Device Regulations 2
G Does anyone know about tobacco-free nicotine pouches? US Food and Drug Administration (FDA) 2
cgaro62 Does FDA apply to a non-medical 13485 certified custom manufacturing company? ISO 13485:2016 - Medical Device Quality Management Systems 11
R Does anyone use iQMS for their ISO based document control? Manufacturing and Related Processes 5
V How many hrs does it take to create a Technical File (TD)? EU Medical Device Regulations 4
M How does FDA determine OAI and VAI after inspection? ISO 13485:2016 - Medical Device Quality Management Systems 0
G Does TPI agencies comes under outsourced process as per Q1 Oil and Gas Industry Standards and Regulations 11
N FPY requested for an industry that does not have rework IATF 16949 - Automotive Quality Systems Standard 4
William55401 21 CFR 11 Password Aging - What does "periodically" revised mean in your org? Qualification and Validation (including 21 CFR Part 11) 3
I CQI-15 Welding System Assessment 2nd edition - Does not require Ultrasonic Welding anymore? Customer and Company Specific Requirements 0
Ajit Basrur Does "Refurbishment" fall under "Service"? ISO 13485:2016 - Medical Device Quality Management Systems 13
T Does marketing company require CE mark if manufacturer has CE mark on product? EU Medical Device Regulations 5
Watchcat REGULATORY WATCHCAT De Novo Post-Mortem 6 – How Does This Even Happen? Other US Medical Device Regulations 0
T What does VW mean by annual requalification? Customer and Company Specific Requirements 4
I Does BSI require suppliers to be ISO 9001 Certified? EU Medical Device Regulations 12
Watchcat Does Regulatory Affairs put the "no" in innovation? Other US Medical Device Regulations 14
Q Does anyone know what this call out means? Manufacturing and Related Processes 3
K COPLANARITY: Composite profile tolerance on multiple surfaces- what does" lower dimensional reference frame tolerance" control? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 11
P Does FDA require certification for quality system internal audit for auditor? Qualification and Validation (including 21 CFR Part 11) 1
H Does anyone has feedback on a notified body for small companies? EU Medical Device Regulations 3
M Does 4.5 - Alternative RISK CONTROL apply to the Particular Standards? IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
E Does IVD need to integrate with hospital IT infrastructure? Medical Information Technology, Medical Software and Health Informatics 2

Similar threads

Top Bottom