Cannot create Rejects for TMV on a medical instrument with an LCD

S

SteHa

#11
I have a bad idea - if the failure mode is one that can be manually induced, you could damage a piece of product accordingly for a test piece.

I could be way off base, but the flaw mode reminds me of damages done to LCDs by pressure, causing bright spots, and by pixel failures, causing .... well, little dots of unintended color or no color.
Hi Normzone,
You're not way off base. What is difficult is causing the failure for specific purpose such as contrast or text corruption (missing or too many segments). We might be causing other failures as well that may cause issues with the test.

We have identified some possibilities for some of the fialure modes as mentioned above and are going to go back to the mfgr to see if they have LCD fall out that we can use.

Appreciate your insight!

Thanks,

Steve
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
C Document Control using Wiki - Cannot Create all Documents as Wiki Pages Document Control Systems, Procedures, Forms and Templates 10
supadrai Possible to Submit a 510(k) if you have never, do not and cannot produce the device for which you're submitting the application? US Food and Drug Administration (FDA) 4
I Cannot Export multiple sections from Excel to PDF without losing pagination Excel .xls Spreadsheet Templates and Tools 23
L How to evaluate the process capability of a data set that is non-normal (cannot be transformed and does not fit any known distribution)? Capability, Accuracy and Stability - Processes, Machines, etc. 12
BradM Cannot stay logged in Elsmar Cove Forum Suggestions, Complaints, Problems and Bug Reports 16
K What is supposed to happen when a CA cannot be closed out or the root cause... General Auditing Discussions 1
insect warfare Cannot determine what type of medical device this product is.... 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
K Anyone who audits 8.2.2 cannot audit other clauses of the standard? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 31
rob73 If NB's (notified bodies) cannot be trusted how can we? EU Medical Device Regulations 39
K Corrective Action cannot be completed within the agreed time frame Nonconformance and Corrective Action 7
X Cannot Verify until Customer uses Product - Clause 7.5.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
L Preventive Action should not / cannot be taken when rectifying a problem ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 94
W What can/cannot be placed on packaging/advertising relating to ISO/TS? Registrars and Notified Bodies 1
M 'Searched' virus? Cannot delete folder - HELP please After Work and Weekend Discussion Topics 33
A Changes to QRI (Quick Reference Instruction)? What I can or cannot change ISO 13485:2016 - Medical Device Quality Management Systems 2
T Control Chart on Paper vs. Software where trend cannot be seen (Alarm only) Statistical Analysis Tools, Techniques and SPC 8
J Is it true that the Quality Manual cannot be a Procedure? Quality Management System (QMS) Manuals 13
C What can I do if I cannot meet PPAP deadline? APQP and PPAP 4
D New thread ring cannot be threaded onto the truncated part of the master General Measurement Device and Calibration Topics 4
E MSA Manual says the sum of EV,AV,GRR, and PV cannot equal 100%? Why? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 2
D Disaster Recovery Plan - I cannot find references to same in ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 3
C What is the best practice to label small tools (small pins) which cannot be scribed? General Measurement Device and Calibration Topics 5
A Goals cannot be reached, don't adjust the goals, adjust the action steps Coffee Break and Water Cooler Discussions 8
Casana Auditor changing ISO 9001 AUDIT scope midstream - Cannot exclude all of 7.3 anymore General Auditing Discussions 26
V MINITAB and non-normal unilateral tolerance data - Cannot confirm Ppk values Using Minitab Software 15
M ISO 9001 Clause 7.6 Measuring Devices cannot be excluded!? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 48
R 17025 Calibration Requirements - External calibration service cannot calibrate ISO 17025 related Discussions 4
T Some Suppliers to TS 16949 companies told they cannot register to TS 16949 IATF 16949 - Automotive Quality Systems Standard 4
Casana Distributors cannot convert to TS? IATF 16949 - Automotive Quality Systems Standard 2
L I looking for a book, but cannot remember the name? . . . . HELP! Book, Video, Blog and Web Site Reviews and Recommendations 3
T Scope and Purpose - For some reason cannot seem to write anything - ISO 9001 - 7.2.2 Document Control Systems, Procedures, Forms and Templates 8
M Gage R&R and Capability - Between 10% and 30% and cannot be improved Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 4
Q Nonconformance vs. Nonconformity - I cannot find major and minor, either! Nonconformance and Corrective Action 36
D ISO 13485 - 7.3.6 Design and development verification - Do most folks create a separate SOP? ISO 13485:2016 - Medical Device Quality Management Systems 6
J Question: How to create an IMDS RoHS, REACH, ELV, IMDS and Restricted Substances 3
M Do we need to create a new CER or can we just update the existing CER EU Medical Device Regulations 3
J Create your own symbol? Other Medical Device Related Standards 7
D How to create IQ, OQ, PQ protocol for existing equipment Other Medical Device Related Standards 2
O How to create robustness checklist from p diagram FMEA and Control Plans 9
T Change control and configuration management - When to create a new model/part number? Other Medical Device and Orthopedic Related Topics 0
R How to create a Work Breakdown Structure? Registrars and Notified Bodies 2
H IMDS for material - Can my Customer create one for my material? RoHS, REACH, ELV, IMDS and Restricted Substances 4
A How do I create a 3^k factorial design with factors be treated as continuous where I Using Minitab Software 0
E How do I create a FMEA for the Internal Audit process? Internal Auditing 11
S Response Surface Method to create design matrix in Minitab Using Minitab Software 5
RoxaneB Carte Blanche to Create an Audit Programme General Auditing Discussions 5
O Is it "legit" to create IMDS before Part Production? RoHS, REACH, ELV, IMDS and Restricted Substances 4
G How to create a mixed OAs in Minitab Using Minitab Software 1
S How to create an Audit Checklist using a Turtle Diagram Internal Auditing 9
A Could I create company specific Employee Records? Records and Data - Quality, Legal and Other Evidence 5

Similar threads

Top Bottom