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Composite Respiratory Kit: Nationwide Medical

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Composite Respiratory Kit: Nationwide Medical FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
Composite Respiratory Kit: Nationwide Medical 6-0556B, 1-0021B, 1-0014B, 1-0027B, 1-No Smoking Sign, 1-0590B, 1-Cylinder Wrench FDA UDI
Model / Reference
0837 FDA UDI
Description
Composite Respiratory Kit: Nationwide Medical 6-0556B, 1-0021B, 1-0014B, 1-0027B, 1-No Smoking Sign, 1-0590B, 1-Cylinder Wrench FDA UDI

Identifiers

Primary DI / UDI-DI
00709078002595 FDA UDI
FDA Product Code
CAT FDA UDI
BYX FDA UDI
CAW FDA UDI
GMDN Term
Oxygen administration tubing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 FDA UDI
868.5860 FDA UDI
868.5440 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal oxygen cannula, carbon-dioxide-samplingOxygen administration tubingOxygen administration kitBreathing circuit condensate trap, reusable

Composite Respiratory Kit: Nationwide Medical by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing circuit condensate trap, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 33e01839-e3e3-4b61-9808-8680bd02b3d8 33 fields · synced May 30, 2026