Meridian Ag

FDA Filings

This page includes the latest FDA filings for Meridian Ag. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number8030988
FEI Number3003282815
NameMERIDIAN AG
Owner & OperatorMERIDIAN AG
Contact AddressBIERIGUTSTRASSE 7 --
THUN CH-NOTA CH-3608 CH
US Agent
Importing Logistics Registration
ImporterPhoenix Research Laboratories
Address6920 Koll Center Pkwy Suite 219
Pleasanton, CA 94566 UNITED STATES
Importer TypeImporter for pre clinical tests in l
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressBIERIGUTSTRASSE 7
THUN Bern, CH-3608 CH
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
MERIDIAN AG
MICRORUPTOR 62017-05-19
MERIDIAN AG
Laser Indirect Ophthalmoscope 500 (LIO-500)2012-05-02
MERIDIAN AG
LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)2012-02-14
MERIDIAN AG
Merilas 532alpha2008-03-12
MERIDIAN AG
Microruptor V2008-03-12
MERIDIAN AG
MRV2008-03-12
MERIDIAN AG
MERILAS 532A2007-12-14
MERIDIAN AG
MICRORUPTER V2002-09-26
MERIDIAN AG
LASAG MICRORUPTOR III Q-SWITCH ND:YAG1991-04-05
MERIDIAN AG
LASAG TOPAZ ND:YAG LASER SYSTEM1990-05-01
MERIDIAN AG
MICRORUPTOR MR-2 ND:YAG LASER SYSTEM1988-10-26
MERIDIAN AG
MICRORUPTOR MR-2 ND:YAG LASER SYSTEM1987-08-27
MERIDIAN AG
MICRORUPTOR MR-2 ND:YAG LASER SYSTEM1987-06-22
MERIDIAN AG
MICRORUPTOR MR-2 ND:YAG LASER SYSTEM1986-05-30
MERIDIAN AG
MICRORUPTOR MR-2 ND:YAG LASER SYSTEM1986-01-31

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