Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003961883

FEI Number

3003961883

Entity Name

INTERLAB S.R.L.

City/State/Country

ROME Lazio, IT

Establishment Address

VIA RINA MONTI N.26, ROME Lazio 00155, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SEBIA (Owner Number: 8023024)

Owner / Operator Contact Address

PARC TECHNOLOGIQUE LEONARD DE, 27 rue Leonard de VINCI, Lisses-Evry, FR-NOTA 91008, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K103757

PMA Number

N/A

All Registered Proprietary Names

Interlab G26 Electrophoresis System Immunofixation Electrophoresis

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DFH	Kappa, Antigen, Antiserum, Control	Immunology	Class 2	866.5550	2016-12-05
CEF	Electrophoretic, Protein Fractionation	Clinical Chemistry	Class 1	862.1630	2016-12-05
DEH	Lambda, Antigen, Antiserum, Control	Immunology	Class 2	866.5550	2016-12-05
CFF	Immunoelectrophoretic, Immunoglobulins, (G, A, M)	Immunology	Class 2	866.5510	2016-12-05

Official Correspondent

Arnaud Collin

US Agent Details

Karen Anderson Business: Sebia Email: karen.anderson@sebia-usa.com Phone: (770) 4463707

Related Public Records

Same Entity

SEBIA

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
8023024	SEBIA	EVRY Essonne, FR

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K822676	Amico Lab, Inc.	FITC ANTISERA TO HUMAN IGG	1982-11-17

Similar Registrations

Registration Number	Establishment Name	Location
2050010	BECKMAN COULTER, INC.	CARLSBAD, CA, US
2083566	THE BINDING SITE, INC.	SAN DIEGO, CA, US
3012471076	THE BINDING SITE	Kings Norton Birmingham, GB
9610806	Siemens Healthcare Diagnostics Products GmbH	MARBURG Hesse, DE
8023024	SEBIA	EVRY Essonne, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003961883. Last updated year: 2026. Please use registration number 3003961883 when referencing this establishment in official correspondence.