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Respiratory Accessory

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Respiratory Accessory FDA UDI
Generic Name
Artificial airway cuff inflation tubing FDA UDI
Device Name
Oxygen Enrichment Adaptor 22mm O.D. x 22mm O.D./15mmI.D. with 6mm Barbed Rotating Stem - WITH CAP - 1/pk FDA UDI
Model / Reference
RES019-CAP1 FDA UDI
Description
Oxygen Enrichment Adaptor 22mm O.D. x 22mm O.D./15mmI.D. with 6mm Barbed Rotating Stem - WITH CAP - 1/pk FDA UDI

Identifiers

Primary DI / UDI-DI
00848530099718 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Artificial airway cuff inflation tubing

Respiratory Accessory 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 ca658641-4cf4-4a72-bb32-b5c06799a061 34 fields · synced May 30, 2026