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Oxygen Connector

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Oxygen Connector FDA UDI
Generic Name
Artificial airway cuff inflation tubing FDA UDI
Device Name
7ft Oxygen Supply Tube FDA UDI
Model / Reference
RES3007Z FDA UDI
Description
7ft Oxygen Supply Tube FDA UDI

Identifiers

Primary DI / UDI-DI
00848530097080 FDA UDI
FDA Product Code
BZA FDA UDI
GMDN Term
Artificial airway cuff inflation tubing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5810 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: Artificial airway cuff inflation tubing

Oxygen Connector by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Artificial airway cuff inflation tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f6bc588e-4e94-4efc-af17-276406c75914 34 fields · synced Jun 8, 2026