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Nebulizer Kit

FDA UDI

Class II (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Nebulizer Kit FDA UDI
Generic Name
Nebulizing system delivery set, single-use FDA UDI
Device Name
Disposable Nebulizer Kit with T-Piece, Jet Nebulizer, 7ft O2 Tubing - 5/pack FDA UDI
Model / Reference
ARES110RES091-5 FDA UDI
Description
Disposable Nebulizer Kit with T-Piece, Jet Nebulizer, 7ft O2 Tubing - 5/pack FDA UDI

Identifiers

Primary DI / UDI-DI
00789091681588 FDA UDI
510(k) Number
K091272 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nebulizing system delivery set, single-use

Nebulizer Kit by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 124e63e8-7c1e-4fec-8cce-8c17d22cb3b7 35 fields · synced Jun 8, 2026