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Fox Mobile

FDA UDI

Class II (US FDA UDI)

by Vectura Group Plc

Identity

Trade Name
FOX MOBILE FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Device Name
The Nebuliser Mouthpiece is part of the FOX MOBILE Inhalation Set. FDA UDI
Model / Reference
Nebuliser Mouthpiece FDA UDI
Description
The Nebuliser Mouthpiece is part of the FOX MOBILE Inhalation Set. FDA UDI

Identifiers

Catalog Number
08CD0002 FDA UDI
Primary DI / UDI-DI
05056143200000 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Therapeutic agent nebulizer, benchtop FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Therapeutic agent nebulizer, benchtop

Fox Mobile by Vectura Group Plc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Therapeutic agent nebulizer, benchtop.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vectura Group Plc

Sources (1)

  • FDA UDI 5166144e-6f2f-420a-b559-f942852f3e0f 35 fields · synced Jun 8, 2026