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Adult Nebulizer Kit

FDA UDI

Class I (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
Adult Nebulizer Kit FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Device Name
NEBULIZER VIXONE ADULT AEROSOL MASK 7' SAFLO OXYGEN TUBING FDA UDI
Model / Reference
MS-6420S FDA UDI
Description
NEBULIZER VIXONE ADULT AEROSOL MASK 7' SAFLO OXYGEN TUBING FDA UDI

Identifiers

Catalog Number
MS-6420S FDA UDI
Primary DI / UDI-DI
00628725097732 FDA UDI
FDA Product Code
CCQ FDA UDI
GMDN Term
Therapeutic agent nebulizer, benchtop FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Therapeutic agent nebulizer, benchtop

Adult Nebulizer Kit by Canadian Hospital Specialties Limited — Class I — 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
Canadian Hospital Specialties Limited

Sources (1)

  • FDA UDI 033cd628-1c19-4049-bf0c-5d9dcbc1a4ab 35 fields · synced Jun 8, 2026