HUDI PHARMA SRL

FDA Device Registration & Listing · Milano, IT · Registration 3015686320

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
3015686320
FEI Number
3015686320
Entity Name
HUDI PHARMA SRL
City/State/Country
Milano, IT
Establishment Address
Piazza Giuseppe Grandi 19, Milano 20129, IT
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
HUDI PHARMA SRL (Owner Number: 10095795)
Owner / Operator Contact Address
Piazza Giuseppe Grandi 19, Milano, IT-MI 20129, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K260007
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2026-04-30

Official Correspondent

Marco Mattielli

US Agent Details

Emily Matorin Business: FDA Basics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

HUDI PHARMA SRL
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
K050212 Qualis, Inc. PERSONAL WARMING JELLY 2005-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015686320. Last updated year: 2026. Please use registration number 3015686320 when referencing this establishment in official correspondence.
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