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Thora-Seal

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Thora-Seal FDA UDI
Generic Name
Chest-percussion airway secretion-clearing system FDA UDI
Device Name
Thora-Seal Chest Drainage Unit Three Chamber System, Collection, Underwater Seal and Suction Control Chambers 2500 mL FDA UDI
Model / Reference
8884713308 FDA UDI
Description
Thora-Seal Chest Drainage Unit Three Chamber System, Collection, Underwater Seal and Suction Control Chambers 2500 mL FDA UDI

Identifiers

Catalog Number
8884713308 FDA UDI
Primary DI / UDI-DI
10192253002652 FDA UDI
FDA Product Code
KDQ 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

Dimensions & Sizes

Size
Total Volume — 2500 Milliliter FDA UDI

Category: Chest-percussion airway secretion-clearing system

Thora-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 219ad419-2fda-4a49-b355-d0c5f6882e90 35 fields · synced Jun 8, 2026