what is budi di and how is it used in eudamed udi submissions?
Published 3 years ago • 1.3K plays • Length 4:53Download video MP4
Download video MP3
Similar videos
-
3:54
reed tech insights -- intro to eudamed basic udi di
-
1:49
coffee talk with reed tech - question about gmdn and budi di in eu
-
3:31
what is udi labeling for medical devices
-
8:55
the 4 c's of eudamed udi and device registration
-
6:41
us fda class i udi requirements and exceptions
-
1:51:55
udi – gudid: what medical device manufacturers need to know
-
14:32
what is udi and what to know about sept 2022 fda class i preparation
-
1:00:13
understanding eu eudamed global requirements and gdsn
-
42:19
eudamed secrets with richard houlihan (medical device regulation)
-
1:03:41
how to create your udi with sylvia reingardt from gs1
-
1:08:14
how and when to register eu medical devices and report udi information to eudamed
-
1:30:28
udi gudid webinar from reed tech and the medical devices group
-
1:04:05
webinar recording reed tech and prisym id xtalks feb 20 2020
-
44:48
implementing a global unique device identification (udi) solution: regional update and requirements
-
6:15
eudamed modules and timeline
-
5:31
south korea udi update
-
57:59
linkedin replay - how to place your udi on medical devices
-
2:52
basic udi-di (english version)
-
1:34:45
unique device identification udi requirements and timelines
-
1:06:24
udi challenges and opportunities
-
30:09
udi: 101