← Back to catalogue

Kenorex

FDA UDI

Class II (US FDA UDI)

by Kentron Health Care, Inc.

Identity

Trade Name
KENOREX FDA UDI
Generic Name
Nebulizing system delivery set, single-use FDA UDI
Device Name
NEBULIZER WITH CHILD OXYGEN MASK AND OXYGEN TUBING FDA UDI
Model / Reference
333761 FDA UDI
Description
NEBULIZER WITH CHILD OXYGEN MASK AND OXYGEN TUBING FDA UDI

Identifiers

Catalog Number
333761 FDA UDI
Primary DI / UDI-DI
10852244007324 FDA UDI
510(k) Number
K091272 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, single-use 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Nebulizing system delivery set, single-use

Kenorex by Kentron Health Care, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b6116bf0-263e-4511-9e08-5ee1f1b4d7ac 35 fields · synced May 30, 2026