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MVA1 Viproxy

FDA UDI

Class I (US FDA UDI)

by Cavagna Group Spa

Identity

Trade Name
MVA1 Viproxy FDA UDI
Generic Name
Respiratory oxygen therapy system FDA UDI
Device Name
Valve with Integrated Pressure Regulator for Medical Gas FDA UDI
Model / Reference
MVA1 Viproxy FDA UDI
Description
Valve with Integrated Pressure Regulator for Medical Gas FDA UDI

Identifiers

Catalog Number
MVA1MMX007 FDA UDI
Primary DI / UDI-DI
00850021133016 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

MVA1 Viproxy 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 dd16362d-e3bb-493b-851b-a7ad571d57b9 35 fields · synced May 30, 2026