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Deluxe Tubing Wrap

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Deluxe Tubing Wrap FDA UDI
Generic Name
Aerosol delivery tubing FDA UDI
Device Name
6ft Nylon CPAP Tubing Wrap FDA UDI
Model / Reference
CAP2002 FDA UDI
Description
6ft Nylon CPAP Tubing Wrap FDA UDI

Identifiers

Catalog Number
CAP2002 FDA UDI
Primary DI / UDI-DI
00848530020057 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Aerosol delivery tubing 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

No

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: Aerosol delivery tubing

Deluxe Tubing Wrap by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aerosol delivery tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8d73eb09-7033-4daa-9f7f-fde665491e9f 35 fields · synced Jun 1, 2026