← Back to catalogue

BD Heimlich Valve

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Heimlich Valve FDA UDI
Generic Name
Pleural catheter FDA UDI
Device Name
VALVE HEIMLICH S/SU CHEST DRAINAGE FDA UDI
Model / Reference
373460 FDA UDI
Description
VALVE HEIMLICH S/SU CHEST DRAINAGE FDA UDI

Identifiers

Catalog Number
373460 FDA UDI
Primary DI / UDI-DI
50382903734608 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Pleural catheter 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: Pleural catheter

BD Heimlich Valve by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pleural catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 3fe132e7-09ae-4946-8da3-d7754967496d 35 fields · synced May 30, 2026