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PleurX

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc.

Identity

Trade Name
PleurX FDA UDI
Generic Name
Pleural/peritoneal drainage catheterization kit FDA UDI
Device Name
PleurX Valve Cap FDA UDI
Model / Reference
50-7235 FDA UDI
Description
PleurX Valve Cap FDA UDI

Identifiers

Catalog Number
50-7235 FDA UDI
Primary DI / UDI-DI
10885403090684 FDA UDI
FDA Product Code
DWM FDA UDI
PNG FDA UDI
GMDN Term
Pleural/peritoneal drainage catheterization kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5050 FDA UDI
876.5630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

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/peritoneal drainage catheterization kit

PleurX by Carefusion 2200, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pleural/peritoneal drainage catheterization kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Carefusion 2200, Inc.

Sources (1)

  • FDA UDI 079d1df6-4379-44b8-995b-2b3852fb4452 35 fields · synced Sep 18, 2026