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H*VENT Vented Chest Seal Two-Pack

FDA UDI

Class I (US FDA UDI)

by H & H Medical Corporation

Identity

Trade Name
H*VENT Vented Chest Seal Two-Pack FDA UDI
Generic Name
Pneumothorax dressing FDA UDI
Device Name
H&H H*VENT Vented Chest Seal Two Pack, containing two individually packaged vented chest seals for sealing open chest wounds and reducing the risk of tension pneumothorax. FDA UDI
Model / Reference
1 FDA UDI
Description
H&H H*VENT Vented Chest Seal Two Pack, containing two individually packaged vented chest seals for sealing open chest wounds and reducing the risk of tension pneumothorax. FDA UDI

Identifiers

Catalog Number
HVS02 FDA UDI
Primary DI / UDI-DI
00857048006460 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Pneumothorax dressing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pneumothorax dressing

H*VENT Vented Chest Seal Two-Pack by H & H Medical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pneumothorax dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5246bf9d-0e42-4c49-8ff1-0098d97c61d0 35 fields · synced May 30, 2026