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Drive DeVilbiss Vacu-Aide Suction Unit

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Drive DeVilbiss Vacu-Aide Suction Unit FDA UDI
Generic Name
Vacuum-assisted airway secretion-clearing system FDA UDI
Device Name
Vacu-Aide w/battery, North America FDA UDI
Model / Reference
7325P-D FDA UDI
Description
Vacu-Aide w/battery, North America FDA UDI

Identifiers

Catalog Number
7325P-D FDA UDI
Primary DI / UDI-DI
00885304032564 FDA UDI
510(k) Number
K982304 FDA UDI
FDA Product Code
JCX FDA UDI
GMDN Term
Vacuum-assisted airway secretion-clearing system 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Vacuum-assisted airway secretion-clearing system

Drive DeVilbiss Vacu-Aide Suction Unit by Drive Devilbiss Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum-assisted airway secretion-clearing system.

Cleared under the same submission

K982304 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI 9392586e-40e5-47ef-b9b9-54a8bdda97d9 37 fields · synced Jun 8, 2026