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MVA2 Viproxy 1 Touch

FDA UDI

Class I (US FDA UDI)

by Cavagna Group Spa

Identity

Trade Name
MVA2 Viproxy 1 Touch FDA UDI
Generic Name
Respiratory oxygen therapy system FDA UDI
Device Name
Valve with Integrated Pressure Regulator for Medical Gas FDA UDI
Model / Reference
MVA2 Viproxy 1 Touch FDA UDI
Description
Valve with Integrated Pressure Regulator for Medical Gas FDA UDI

Identifiers

Catalog Number
MVA2UOS012 FDA UDI
Primary DI / UDI-DI
00850021133061 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
Respiratory oxygen therapy system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Non-fixed medical gas cylinder regulatorRespiratory oxygen therapy systemFixed medical gas cylinder regulatorFixed-regulator oxygen refillable cylinder

MVA2 Viproxy 1 Touch by Cavagna Group Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixed-regulator oxygen refillable cylinder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cavagna Group Spa

Sources (1)

  • FDA UDI c409232c-7438-4bad-a212-8efd91f10e9c 35 fields · synced May 30, 2026