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Portable Suction

FDA UDI

Class II (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Portable Suction FDA UDI
Generic Name
Emergency airway clearance suction pump, electric FDA UDI
Device Name
Sunset Suction Machine Only - with AC Power Only, Detachable Power Cord & Carry Case FDA UDI
Model / Reference
SU100AC-A FDA UDI
Description
Sunset Suction Machine Only - with AC Power Only, Detachable Power Cord & Carry Case FDA UDI

Identifiers

Primary DI / UDI-DI
00848530096199 FDA UDI
FDA Product Code
JCX FDA UDI
GMDN Term
Emergency airway clearance suction pump, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Emergency airway clearance suction pump, electric

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

Similar devices

Also classified as Emergency airway clearance suction pump, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8e897ab7-6d41-4aa3-9369-4024f4435176 34 fields · synced May 31, 2026