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Aqua-Seal

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Aqua-Seal FDA UDI
Generic Name
Chest-percussion airway secretion-clearing system FDA UDI
Device Name
Chest Drainage Unit,Wet Suction FDA UDI
Model / Reference
8888571299 FDA UDI
Description
Chest Drainage Unit,Wet Suction FDA UDI

Identifiers

Catalog Number
8888571299 FDA UDI
Primary DI / UDI-DI
10192253003017 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Chest-percussion airway secretion-clearing system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Chest-percussion airway secretion-clearing system

Aqua-Seal by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chest-percussion airway secretion-clearing system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 8c8282d3-bd23-4fd4-b87b-b59fb79bfc3b 34 fields · synced Jun 8, 2026