SANICOT SRL

FDA Device Registration & Listing · Prato, IT · Registration 3013960742

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
3013960742
FEI Number
3013960742
Entity Name
SANICOT SRL
City/State/Country
Prato, IT
Establishment Address
Via Martino Meucci 21, Prato 59100, IT
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Sanicot srl (Owner Number: 10058527)
Owner / Operator Contact Address
Via Martino Meucci 21, Prato, IT-PO 59100, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
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
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2018-10-07

Official Correspondent

Deborah Pierozzi

US Agent Details

Massimiliano Bardin Business: Corman USA Inc Email: massimiliano.bardin@corman.it Phone: (917) 2153647

Related Public Records

Same Entity

Sanicot 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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013960742. Last updated year: 2026. Please use registration number 3013960742 when referencing this establishment in official correspondence.
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