Veterinary Use device regulation - Serbia, EU and Switzerland

M

MD_Simy86

#1
#1
Dear all,
I'm looking for some information regarding devices with veterinary use regulation in the following Countries:

- European Union;
- Serbia;
- Switzerland

Does anyone know anything about this issue in these Countries?

Plaese answer me as soon as possible for you,
bye bye:bigwave::bigwave:
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
O Unique situation regarding a Veterinary Medical Device and ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 4
M Veterinary Medical Device Registration in the EU and Italy EU Medical Device Regulations 6
C FDA Approval Process for Device that can also be used for Veterinary Purpose 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
L Veterinary device is medical device or not? ISO 13485:2016 - Medical Device Quality Management Systems 15
R X-RAY Based Diagnostic Veterinary medical Devices Medical Device and FDA Regulations and Standards News 2
GoSpeedRacer Veterinary anesthesia machine CE Marking (Conformité Européene) / CB Scheme 1
D Internal audit forms or checklists for a medical/veterinary laboratory General Auditing Discussions 5
M Veterinary Medical Devices - Glucose monitoring system EU Medical Device Regulations 4
O Panama - Veterinary Diagnostics Other Medical Device Regulations World-Wide 1
M Veterinary Devices - CE Marking Categories CE Marking (Conformité Européene) / CB Scheme 6
E INDONESIA: Regulatory Requirements for Veterinary x-ray equipment Other Medical Device Regulations World-Wide 2
K Regulations for sending Veterinary Surgical Instruments to Qatar Other Medical Device Regulations World-Wide 4
S Veterinary Diagnostic Kits Regulations in South East Asia Other Medical Device Regulations World-Wide 8
B IVD Veterinary Testing - European Market Regulations Other ISO and International Standards and European Regulations 6
N Sterilisation of IV Bags used for Veterinary Blood Plasma Products ISO 13485:2016 - Medical Device Quality Management Systems 7
somashekar Regulatory and Safety Standards for Veterinary Medical Devices Other Medical Device Related Standards 10
L How to sell Veterinary Devices to Canada Canada Medical Device Regulations 5
M Changing Investigational Device from Non-Sterile to Sterile - what are the implications? Other Medical Device and Orthopedic Related Topics 3
B FDA Breakthrough Device can be overlapped with a designated device? US Food and Drug Administration (FDA) 6
D Add new device to current license Canada Medical Device Regulations 0
S Obsolescence of the Medical Device in Various Countries Other Medical Device Related Standards 0
A MDR - Legacy Device Review Timeframe and Requirements EU Medical Device Regulations 3
A IT-NETWORK in PEMS Sub-Clause 14.13 for Medical Device IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
G Medical Device - Borderline/Definition EU Medical Device Regulations 0
B Is labeling on the device itself required? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
A Intended Purpose on device label EU Medical Device Regulations 7
S Medical device equipment calibration Qualification and Validation (including 21 CFR Part 11) 1
P European Medical Device Nomenclature (EMDN) and CND EU Medical Device Regulations 3
S Reseller Request to Change UPC on Medical Device via Re-labeling Medical Device and FDA Regulations and Standards News 5
D Hand Held medical device - power supply requirements IEC 60601 - Medical Electrical Equipment Safety Standards Series 7
T CE Marking - Bench mark Device from same manufacturer CE Marking (Conformité Européene) / CB Scheme 2
E Medical device applicability to WEEE Other ISO and International Standards and European Regulations 2
Fjalar Spare parts for discontinued MDD compliant class I medical device EU Medical Device Regulations 4
H Medical Device Label Acceptance Criteria Manufacturing and Related Processes 4
J Calling a medical device a medical device (when it might not be one..) UK Medical Device Regulations 29
B Regulatory Affairs Certification (RAC) Book - Fundamentals of Medical Device Regulations Medical Device and FDA Regulations and Standards News 0
A How can we change a device trade name in 510(k) summary? US Food and Drug Administration (FDA) 0
N Medical device name in different countries EU Medical Device Regulations 4
M Issues with leakage current testing for a CLASS II device since no PE and FE is present IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
V Medical Device Literature Translation Software ISO 13485:2016 - Medical Device Quality Management Systems 1
M Are you allowed to reuse the same asset number if the device was replaced? General Measurement Device and Calibration Topics 10
G ISO 13485 Certification - Can we get the ISO 13485 certification prior to shipment of the device? ISO 13485:2016 - Medical Device Quality Management Systems 6
J Med Device Class for a Service Organization ISO 13485:2016 - Medical Device Quality Management Systems 2
Z Over The Air (OTA) updates for medical device Other US Medical Device Regulations 1
H Tukery Medical Device Regulstion Other Medical Device Regulations World-Wide 0
J UDI-DI how should we interpret Device version or model to determine if a new UDI-DI is needed? EU Medical Device Regulations 0
T Device & Accessory, Components in device, or System EU Medical Device Regulations 0
shimonv Clinical evaluation report for class I device EU Medical Device Regulations 3
P UDI-PI requirements on reusable surgical device, do we need serialisation? ISO 13485:2016 - Medical Device Quality Management Systems 3
M Medical device certificate in Australia - ARTG certificate Other Medical Device Regulations World-Wide 0

Similar threads

Top Bottom