Araymondlife

FDA Filings

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

FDA Registration(s)
Registration Number3011392709
FEI Number3011392709
NameARAYMONDLIFE
Owner & OperatorARAYMONDLIFE
Contact Address1 RUE LOUIS BESANCON
SAINT-EGREVE FR-38 Isere 38120 FR
Official Correspondent
  • MAXIME BONNET
  • 33-4-5738122-6
US Agent
Importing Logistics Registration
ImporterMylan Laboratories Limited
650658052
AddressHosur Steriles Facility, Plot # 13 A,14, CP2 SIPCOT-II Krishnagiri Main Road
HOSUR, 635130 INDIA
Phone91 4344 661400
SubdivisionIN-TN
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1 RUE LOUIS BESANCON
SAINT-EGREVE Isere, 38120 FR
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Export Device to the United States But Perform No Other Operation on Device

FDA Filings

Device
Company
DeviceDate
ARAYMONDLIFE
VIAL ADAPTER FOR RAYDYLYO2020-03-05
ARAYMONDLIFE
STERILE DISPOSABLE GUIDE2018-09-03

Related Finance Registrations
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.