Medical device equipment calibration

sharonblon88

Starting to get Involved
#1
May I know if the equipment calibration service can be online? It's hard to find calibration service at local for respirator tester calibration. And most equipment is from oversea. Or do you know any calibration service companies provide service in california?
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
P Manufacturing equipment (e.g.: Dental Welder): medical device or not? US Food and Drug Administration (FDA) 5
D Medical device development - Custom test equipment ISO 13485:2016 - Medical Device Quality Management Systems 4
E Multiple socket-outlets - Medical Device Electrical Equipment IEC 60601 - Medical Electrical Equipment Safety Standards Series 12
L Medical Device Manufacturing Equipment Design Other Medical Device Related Standards 2
T What is Medical Device Classification for diagnostic equipment in ASEAN ? Other Medical Device Regulations World-Wide 2
thisby_ Medical Device Battery Powered Equipment connected to Charger IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
W Medical Device Manufacturer Demonstration Equipment Other US Medical Device Regulations 6
E Does R&D Equipment in Medical Device Industry require IQ/OQ Qualification and Validation (including 21 CFR Part 11) 9
E Is our equipment a Medical Device under US regulation ? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 9
J Confused about application of ISO 13485 - Manufacturer of Medical Equipment & Device ISO 13485:2016 - Medical Device Quality Management Systems 14
G Old Medical Device Equipment - Compliance with New or Old Standard - What to do? Other Medical Device Related Standards 3
C Safe Handling of Non-Device Refurbished Medical Equipment US Food and Drug Administration (FDA) 3
C Labeling requirements when selling demo Medical Device equipment 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
H Cooling Equipment Qualification for Medical Device Manufacturing EU Medical Device Regulations 3
S Medical Device Battery Powered Equipment with Battery Charger Classification IEC 60601 - Medical Electrical Equipment Safety Standards Series 17
P Medical Device OEM (Original Equipment Manufacturer) Agreements Other Medical Device and Orthopedic Related Topics 5
R Equipment Cleaning Validation Requirements - Medical Device Class II or Class III Other Medical Device and Orthopedic Related Topics 5
M Process Validation/Equipment Qualification - Class 1A (Sterile) Medical Device ISO 13485:2016 - Medical Device Quality Management Systems 12
W Software development company for Medical Device Diagnostic Equipment ISO 13485:2016 - Medical Device Quality Management Systems 5
M FDA Medical device reporting (Manufacturer in US; contract manufacturer OuS) US Food and Drug Administration (FDA) 0
G Medical Device Auditor (CMDA) certification exam by ASQ - looking for input Career and Occupation Discussions 3
B Documenting Medical Device Complaints after End of Life? Medical Device and FDA Regulations and Standards News 0
M Medical Device License as Distributor Canada Medical Device Regulations 8
M Preparing a document for Raw Material of Medical Device EU Medical Device Regulations 1
R Medical device regulations in African countries Other Medical Device Regulations World-Wide 0
Z Swiss Authorized representative & non-medical device regulations Other Medical Device Regulations World-Wide 0
T FDA UDI Question - Class II Medical Device Other US Medical Device Regulations 1
blackholequasar ISO 13485 certification prior to Medical Device Manufacturing... worth it? ISO 13485:2016 - Medical Device Quality Management Systems 4
P Brexit Germany - Import Medical Device For Clinical Study EU Medical Device Regulations 0
M Medical Device Marketing Material - Control of Social Media 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
Ed Panek Make sure you hire competent QA RA Folks before making a "Medical Device." Coffee Break and Water Cooler Discussions 1
B Acquired Medical Device Product Line - Documentation Requirements for Device Master Record ISO 13485:2016 - Medical Device Quality Management Systems 7
MedicalDevicesCanada How to find a medical device contract manufacturer, MDSAP certified? Canada Medical Device Regulations 4
dgrainger Informational MHRA's Software and AI as a Medical Device Change Programme UK Medical Device Regulations 0
S Medical Device - Technical Documentation structure EU Medical Device Regulations 1
LostLouie Archived Specifications and Drawings for Medical Device Technical Files EU Medical Device Regulations 4
B Reprocessing of an accessory for a medical device EU Medical Device Regulations 4
A Class 1 medical device - Thailand Other Medical Device Regulations World-Wide 0
P Interchangeable/alternative parts in BOM (medical device) Manufacturing and Related Processes 4
U Is Initial Importer Status Required if a Medical Device is Manufactured and Sterilized by an OEM in the US Other US Medical Device Regulations 1
J Shoe Covers - medical device class I EU Medical Device Regulations 3
J Software as a Medical Device - SaMD IEC 62304 - Medical Device Software Life Cycle Processes 3
C CE Marking - Medical Device Accessories EU Medical Device Regulations 0
H Existing cloud based medical device - questions regarding improving the processes IEC 62304 - Medical Device Software Life Cycle Processes 6
K Unused Service Parts in Newly Manufactured Medical Device? Other US Medical Device Regulations 1
B A.I. diagnostic software is considered as medical device in FDA? US Food and Drug Administration (FDA) 6
J Medical device repairs (to upholstery) Manufacturing and Related Processes 4
Ed Panek Apple Provides New Medical Device Cautions 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
C Does a medical device active (zinc oxide) needs BPR registration in EU? Other ISO and International Standards and European Regulations 5
DanBOS Cloud Connected Medical Device 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3

Similar threads

Top Bottom