FARMA-DERMA S.R.L.

FDA Device Registration & Listing · SALA BOLOGNESE Bologna, IT · Registration 3013474580

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
3013474580
FEI Number
3013474580
Entity Name
FARMA-DERMA S.R.L.
City/State/Country
SALA BOLOGNESE Bologna, IT
Establishment Address
VIA DELL'ARTIGIANO 6-8, SALA BOLOGNESE Bologna 40010, IT
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
FARMA-DERMA S.r.l. (Owner Number: 10056612)
Owner / Operator Contact Address
VIA DELL'ARTIGIANO 6-8, SALA BOLOGNESE, IT-BO 40010, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K213220
PMA Number
N/A

All Registered Proprietary Names

REVAREE PLUS VAGINAL SUPPOSITORIES

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2023-07-25

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

FARMA-DERMA S.r.l.
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 3013474580. Last updated year: 2026. Please use registration number 3013474580 when referencing this establishment in official correspondence.
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