Interlab S R L

FDA Filings

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

FDA Registration(s)
Registration Number3003961883
FEI Number3003961883
NameINTERLAB S.R.L.
Owner & OperatorSEBIA
Contact AddressPARC TECHNOLOGIQUE LEONARD DE 27 rue Leonard de VINCI
Lisses-Evry FR-NOTA 91008 FR
Official Correspondent
  • Arnaud - Collin
  • 33-169-898331-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressVIA RINA MONTI N.26
ROME Lazio, 00155 IT
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
INTERLAB S.R.L. [SEBIA]
Interlab G26 Electrophoresis System Immunofixation Electrophoresis2016-12-05
INTERLAB S.R.L. [SEBIA]
Interlab G26 Electrophoresis System Immunofixation Electrophoresis2016-12-05
INTERLAB S.R.L. [SEBIA]
Interlab G26 Electrophoresis System Immunofixation Electrophoresis2016-12-05
INTERLAB S.R.L. [SEBIA]
Interlab G26 Electrophoresis System Immunofixation Electrophoresis2016-12-05
INTERLAB S.R.L.
MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM2006-06-30
INTERLAB S.R.L.
INTERLAB ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM2004-05-04
INTERLAB S.R.L.
INTERLAB ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM2004-02-03

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