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Pleur Evac

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PLEUR EVAC FDA UDI
Generic Name
Pleural drainage system FDA UDI
Device Name
Pneumonectomy Drain FDA UDI
Model / Reference
IPN010572 FDA UDI
Description
Pneumonectomy Drain FDA UDI

Identifiers

Catalog Number
A-4301-08LF FDA UDI
Primary DI / UDI-DI
34026704428787 FDA UDI
FDA Product Code
CAC FDA UDI
GMDN Term
Pleural drainage system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5830 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 18 Inch FDA UDI
Depth — 2.5 Inch FDA UDI
Total Volume — 2350 Milliliter FDA UDI
Width — 13 Inch FDA UDI

Category: Pleural drainage system

Pleur Evac by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pleural drainage system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 2a5afbbe-72f3-46e5-98c2-58efa42caee8 36 fields · synced Jun 8, 2026