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Pleur-Evac

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PLEUR-EVAC FDA UDI
Generic Name
Pleural catheter FDA UDI
Device Name
THORACIC CATHETER RIGHT ANGLE 28 FRENCH SOFT FDA UDI
Model / Reference
IPN028458 FDA UDI
Description
THORACIC CATHETER RIGHT ANGLE 28 FRENCH SOFT FDA UDI

Identifiers

Catalog Number
DRAC-28S FDA UDI
Primary DI / UDI-DI
14026704631398 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Pleural catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

Dimensions & Sizes

Size
Length — 20.5 Inch FDA UDI

Category: Pleural catheter

Pleur-Evac by Teleflex Incorporated — Class I — 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

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 858be61b-5d7f-471e-9687-0f82b5de467a 36 fields · synced Jun 1, 2026