ROVIPHARM

FDA Device Registration & Listing · Val Revermont Ain, FR · Registration 3005724348

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
3005724348
FEI Number
3005724348
Entity Name
ROVIPHARM
City/State/Country
Val Revermont Ain, FR
Establishment Address
ZA de Lucinges, 86 Route de Plan D eau, Val Revermont Ain F-01370, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Rovipharm (Owner Number: 10027230)
Owner / Operator Contact Address
ZA de Lucinges, 86 Route de Plan D eau, Val Revermont, FR-NOTA F-01370, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dosing Pipettes Droppers Measuring Cups Dosing Cups Dosing Spoons Measuring Spoons Dosing Pipettes + PIBA PP28 PIBA PP28 Press in Bottle Adapter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2008-10-16

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

Rovipharm
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 3005724348. Last updated year: 2026. Please use registration number 3005724348 when referencing this establishment in official correspondence.
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