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CPAP Accessory

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
CPAP Accessory FDA UDI
Generic Name
Luer/Luer linear connector, reusable FDA UDI
Device Name
V-Com Inspiratory comfort for PAP Therapy FDA UDI
Model / Reference
CAP1026C FDA UDI
Description
V-Com Inspiratory comfort for PAP Therapy FDA UDI

Identifiers

Primary DI / UDI-DI
00848530104535 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Luer/Luer linear connector, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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: Luer/Luer linear connector, reusable

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

Similar devices

Also classified as Luer/Luer linear connector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7c5df382-ad7d-407e-a075-ec4db4c77208 34 fields · synced May 30, 2026