Registering Medical Device in Brazil ANVISA - Fee Structure

R

ramkannan13

Dear All,

Registering medical device with Brazil ANVISA, where can I find the cost or the Fees involved for registering, inspection, importing etc.

:thanx:Rk
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
K Registering a Software medical device (SaMD) in China China Medical Device Regulations 5
shimonv The regulatory process for registering a Medical Device in India Other Medical Device Regulations World-Wide 2
N Registering a Class 1 Sterile Medical Device - Currently selling a Non-Sterile 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 10
M Registering a Class II Medical Device with no Predicate Device - FDA 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
C Registering Medical Devices in Australia and New Zealand - ANZTPA Other Medical Device Regulations World-Wide 1
S Anvisa & INMETRO - Registering Non-Electrical Medical Devices in Brazil Other Medical Device Regulations World-Wide 2
A Registering Medical Products in Canada - DIN EN 14971 vs. CAN/CSA-ISO 14971 Canada Medical Device Regulations 5
N Regulations for Registering Medical Devices in South Korea Other Medical Device Regulations World-Wide 6
M Medical Devices Registering (Registration) Procedure in South Africa Other Medical Device Regulations World-Wide 4
T Product Listing (registering medical devices) in Indonesian Market ISO 13485:2016 - Medical Device Quality Management Systems 2
F Contract Manufacturer Registering with the FDA - Medical Devices - 21 CFR 807.20 ISO 13485:2016 - Medical Device Quality Management Systems 11
M Not registering as manufacturer EU Medical Device Regulations 1
J Requirements for registering Alcohol Wipes (70% IPA) in Canada Medical Device and FDA Regulations and Standards News 4
J ISO13485 Certification Scope - Registering a Subset of our Products ISO 13485:2016 - Medical Device Quality Management Systems 9
M FDA Submission Consultancy - Registering and marketing our products in the US 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
K Job Shop - Registering to AS9100 vs. ISO 9001 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 27
K Registering to AS9100 - Already ISO/TS-16949 Registered AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
T Difference between registering as a Lead Auditor with RABQSA vs. IRCA ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 9
R Requirements for Registering and Listing with the FDA 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
A Registering multiple sites to ISO 9001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
M If there is any restriction on the transportation of Used Medical Device (with blood) from Canada to other countries? Canada Medical Device Regulations 1
M If there is any restriction on the transportation of Used Medical Device (with blood) from EU to other countries? EU Medical Device Regulations 0
adztesla Sterile packaging validation for medical device - ASTMD4332 and ISTA2A ISO 13485:2016 - Medical Device Quality Management Systems 3
P On-going stability study requirement for medical device US Food and Drug Administration (FDA) 2
K Medical devices for laymen and necesssary reprocessing Other Medical Device Related Standards 3
N Regulations for Medical Device in Jamaica Other US Medical Device Regulations 0
M Classification of device according to China medical device regulations China Medical Device Regulations 4
M Looking for kindly help... If there is any prohibits from contract manufacturing in US? About SR medical devices US Medical Device Regulations 0
adztesla Design change and Process change Class 3 medical device Medical Device and FDA Regulations and Standards News 2
K New set of medical devices - samples EU Medical Device Regulations 3
M Importing a custom component for our medical device 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
FRA 2 FDA Reusable Vs Single Use Medical Devices in EU Other Medical Device and Orthopedic Related Topics 1
adztesla Adding new supplier/ Medical device design change ISO 13485:2016 - Medical Device Quality Management Systems 2
adztesla Medical device Drawing related change justification Other Medical Device Related Standards 0
O Medical Device With 2 Power Cords IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
Stoic Which medical device companies are using Recombinant Factor C (rFC) instead of Limulus Amebocyte Lysate (LAL) for endotoxin testing? Sustainability, Green Initiatives and Ecology 0
I Commercializing a non medical device software Medical Information Technology, Medical Software and Health Informatics 10
I Non-medical device software Preventive Action and Continuous Improvement 1
C California Prop 65 for medical device labels US Medical Device Regulations 3
adztesla GDP rules- redline drawings in medical device Medical Device and FDA Regulations and Standards News 2
R Instructions for Use supplied with Medical Device Components Medical Device and FDA Regulations and Standards News 4
M Deburring plastic medical device Manufacturing and Related Processes 1
W Training software medical device Medical Device Related Standards 0
S Modification of medical device EU Medical Device Regulations 2
I Commercialize a non-medical product ISO 13485:2016 - Medical Device Quality Management Systems 5
P Do Barcode scanners need validation in Medical device manufacturing? Manufacturing and Related Processes 6
F The use of 4G/Wi-Fi dongles in medical devices IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
B FDA Requirements for medical device to be used for training purposes only US Food and Drug Administration (FDA) 9
L Verification of wireless QoS and coexistence during FDA certification of medical devices Medical Device and FDA Regulations and Standards News 1
F Adding wireless communication to existing medical device IEC 60601 - Medical Electrical Equipment Safety Standards Series 4

Similar threads

Top Bottom