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Suction Kit

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Suction Kit FDA UDI
Generic Name
Closed-suction breathing circuit connector/switch FDA UDI
Device Name
(1) RES023AW, (1) RES024L10, (1)RES024S, (1) RES025, (1) BF3812, (1) RES028 FDA UDI
Model / Reference
APMD001SUCTION FDA UDI
Description
(1) RES023AW, (1) RES024L10, (1)RES024S, (1) RES025, (1) BF3812, (1) RES028 FDA UDI

Identifiers

Primary DI / UDI-DI
00848530097677 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Closed-suction breathing circuit connector/switch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 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: Closed-suction breathing circuit connector/switch

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

Similar devices

Also classified as Closed-suction breathing circuit connector/switch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SUNSET HEALTHCARE SOLUTIONS, Inc.

Sources (1)

  • FDA UDI 9f6f69c0-5313-425d-b371-38030f3e4644 34 fields · synced May 31, 2026