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Direct Supply

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Direct Supply FDA UDI
Generic Name
Emergency airway clearance suction pump, electric FDA UDI
Device Name
DS Attendant Aspirator FDA UDI
Model / Reference
DS-ASP FDA UDI
Description
DS Attendant Aspirator FDA UDI

Identifiers

Primary DI / UDI-DI
00092237613566 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Emergency airway clearance suction pump, electric

Direct Supply by Compass Health Brands Corp. — 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 e5f331a9-0d79-4f8c-a2f4-8aa36534ad2e 34 fields · synced May 30, 2026