Menu
Home
Forums
New posts
Search forums
What's new
New posts
All posts
New media
New media comments
Latest activity
Media
New media
New comments
Search media
Resources
Latest reviews
New resources
Search resources
Attachment List
Log in
Register
What's new
Search
Search
Everywhere
Threads
This forum
Search titles only
By:
New posts
Search forums
Menu
Log in
Register
Home
Forums
Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
JavaScript is disabled. For a better experience, please enable JavaScript in your browser before proceeding.
You are using an out of date browser. It may not display this or other websites correctly.
You should upgrade or use an
alternative browser
.
EU Medical Device Regulations
The 3 Medical Device Directives and other applicable regulations related to Medical Devices in the EU (European Union).
Prev
1
…
Go to page
Go
60
61
62
63
64
…
Go to page
Go
176
Next
First
Prev
62 of 176
Go to page
Go
Next
Last
Filters
Show only:
Loading…
B
Procedure packs with non-medical devices
BIORA
Apr 8, 2021
Replies
1
Views
804
Apr 9, 2021
Marc
A
Clinical assessment sample size - Medical device Class IIb implantable (93/42 directive)
Armando_C
Apr 7, 2021
Replies
2
Views
1K
Apr 8, 2021
Armando_C
A
CECP, consultation according to Art 54 MDR
Raisin picker
Apr 1, 2021
Replies
1
Views
867
Apr 8, 2021
Raisin picker
K
25-year lifetime of medical device - document storage period
kormach
Apr 7, 2021
Replies
1
Views
815
Apr 7, 2021
shimonv
Notified Body Substantial Change MDD
Ed Panek
Apr 6, 2021
Replies
1
Views
844
Apr 6, 2021
shimonv
M
Sample record for verification performed by importers before placing a device on the market
MDRResearcher
Apr 6, 2021
Replies
0
Views
512
Apr 6, 2021
MDRResearcher
M
P
Requirements for being an European Representative
primavesvera
Apr 5, 2021
Replies
3
Views
679
Apr 6, 2021
twanmul
T
M
FDA or CE requirements for periodic checks of data backups and retrievals
mikezv
Feb 1, 2018
Replies
4
Views
3K
Apr 1, 2021
cmeby
C
J
Should a Class 1 medical device with an option to measure body weight be considered Class 1m?
Jolande
Apr 1, 2021
Replies
0
Views
743
Apr 1, 2021
Jolande
J
J
How to keep MDD certificate valid when legal manufacturer has liquidity problem
Jolande
Mar 31, 2021
Replies
0
Views
698
Mar 31, 2021
Jolande
J
A
Reliable sources for following EU medical device regulatory
Annita
Mar 31, 2021
Replies
0
Views
596
Mar 31, 2021
Annita
A
L
Programmer accessories classification
LOGI2004
Mar 29, 2021
Replies
0
Views
621
Mar 29, 2021
LOGI2004
L
M
Sponsor name presented in the test report
Morris Liu
Mar 28, 2021
Replies
4
Views
583
Mar 29, 2021
Morris Liu
M
M
Extension to shelf life of new product under MDR
mchambe1
Mar 23, 2021
Replies
1
Views
1K
Mar 26, 2021
planB
D
MDR and Summary Technical Documentation Files
Device1000
Apr 17, 2018
2
Replies
18
Views
15K
Mar 25, 2021
MDRexpert
M
Prev
1
…
Go to page
Go
60
61
62
63
64
…
Go to page
Go
176
Next
First
Prev
62 of 176
Go to page
Go
Next
Last
You must log in or register to post here.
Home
Forums
Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to the use of cookies.
Accept
Learn more…
Top
Bottom