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Thora-Vent Thoracic Vent

FDA UDI

Class II (US FDA UDI)

by Uresil Corp.

Identity

Trade Name
Thora-Vent Thoracic Vent FDA UDI
Generic Name
Pneumothorax catheter insertion set FDA UDI
Device Name
Thoracic Vent Occlusion Plug FDA UDI
Model / Reference
TVOCP FDA UDI
Description
Thoracic Vent Occlusion Plug FDA UDI

Identifiers

Catalog Number
TVOCP FDA UDI
Primary DI / UDI-DI
00817640020790 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Pneumothorax catheter insertion set 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

Category: Pneumothorax catheter insertion set

Thora-Vent Thoracic Vent by Uresil Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumothorax catheter insertion set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Uresil Corp.

Sources (1)

  • FDA UDI a25e7e24-928d-4626-90d2-6ceaf794a3cc 36 fields · synced Jun 8, 2026