RAND S.p.A.

FDA Device Registration & Listing · MEDOLLA Modena, IT · Registration 3003793891

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
3003793891
FEI Number
3003793891
Entity Name
RAND S.p.A.
City/State/Country
MEDOLLA Modena, IT
Establishment Address
VIA STATALE 12, 62, MEDOLLA Modena 41036, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
RAND S.p.A. (Owner Number: 9063301)
Owner / Operator Contact Address
VIA STATALE 12, 62, --, MEDOLLA, IT-MO 41036, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K161613
PMA Number
N/A

All Registered Proprietary Names

Ch24 round silicone catheter HANG&GO HT BASIC PERFORMER HT Hang&Go PAC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GBX Catheter, Irrigation General, Plastic Surgery Class 1 878.4200 2012-10-31
LGZ Warmer, Thermal, Infusion Fluid General Hospital Class 2 880.5725 2012-05-18
LGZ Warmer, Thermal, Infusion Fluid General Hospital Class 2 880.5725 2017-01-04

Official Correspondent

MARIA CRISTINA VACCARI

US Agent Details

Silvia Tamarri Business: THEMA CORP Email: usreg@complifegroup.com Phone: (215) 8459459

Related Public Records

Same Entity

RAND S.p.A.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003793891. Last updated year: 2026. Please use registration number 3003793891 when referencing this establishment in official correspondence.
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