Cavagna Group S.p.A - Divisione Omeca

FDA Device Registration & Listing · Ponte San Marco di Calcinato Brescia, IT · Registration 3004145585

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
3004145585
FEI Number
3004145585
Entity Name
Cavagna Group S.p.A - Divisione Omeca
City/State/Country
Ponte San Marco di Calcinato Brescia, IT
Establishment Address
Via Statale No 11/13, Ponte San Marco di Calcinato Brescia 25011, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Cavagna Group S.p.A - Divisione Omeca (Owner Number: 10038986)
Owner / Operator Contact Address
Via Statale No 11/13, PONTE S. MARCO- CALCINATO, IT-BS 25011, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VIPROXY 1touch Viproxy MVB2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAN Regulator, Pressure, Gas Cylinder Anesthesiology Class 1 868.2700 2011-11-30

Official Correspondent

No official correspondent registered.

US Agent Details

Daniel Kamm Business: Kamm & Associates Email: fda.help.now@gmail.com Phone: (847) 3741727

Related Public Records

Same Entity

Cavagna Group S.p.A - Divisione Omeca
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0037-2010 Airgas Puritan Medical Puritan Medical Unit 1
AGI-2237 Portable 2 Cylinder Manifold Cart, for connecting medical gas cylinders.
Z-0038-2010 Airgas Puritan Medical Puritan Medical Unit 1
AGI-2238 Portable 4 Cylinder Manifold Cart, for connecting medical gas cylinders.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004145585. Last updated year: 2026. Please use registration number 3004145585 when referencing this establishment in official correspondence.
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