S.A.L.F. LABORATORIO FRAMACOLOGICO

FDA Device Registration & Listing · Cenate Scotto Bergamo, IT · Registration 3007685782

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007685782
FEI Number
3007685782
Entity Name
S.A.L.F. LABORATORIO FRAMACOLOGICO
City/State/Country
Cenate Scotto Bergamo, IT
Establishment Address
Via Marconi 2, Cenate Scotto Bergamo 24069, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
S.A.L.F. Spa Laboratorio Farmacologico (Owner Number: 10056182)
Owner / Operator Contact Address
Via Marconi 2, Cenate Scotto, IT-BG 24069, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K190063
PMA Number
N/A

All Registered Proprietary Names

S.A.L.F.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2021-11-03
KDL Set, Perfusion, Kidney, Disposable Gastroenterology, Urology Class 2 876.5880 2022-01-04
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2023-11-22
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2018-07-26
MSB System And Accessories, Isolated Heart, Transport And Preservation Gastroenterology, Urology Class 2 876.5880 2019-09-06

Official Correspondent

Carmelo Gagliano

US Agent Details

John Bruens Bruens Business: Global Transplant Solutions, Inc. Email: jbruens@1gtsinc.com Phone: (864) 5926311

Related Public Records

Same Entity

S.A.L.F. Spa Laboratorio Farmacologico
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K013575 Organ Recovery Systems, Inc. KPS-I, THE KIDNEY PERFUSION SOLUTION 2002-01-25

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007685782. Last updated year: 2026. Please use registration number 3007685782 when referencing this establishment in official correspondence.
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