← Back to catalogue

Pleur-Evac

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PLEUR-EVAC FDA UDI
Generic Name
Luer/Luer linear connector, single-use FDA UDI
Device Name
PLEUR EVAC PATIENT TUBING PLUG FDA UDI
Model / Reference
IPN029227 FDA UDI
Description
PLEUR EVAC PATIENT TUBING PLUG FDA UDI

Identifiers

Catalog Number
PE105 FDA UDI
Primary DI / UDI-DI
14026704645326 FDA UDI
FDA Product Code
GCD FDA UDI
GMDN Term
Luer/Luer linear connector, single-use 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 — 2 Inch FDA UDI

Category: Luer/Luer linear connector, single-use

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

Similar devices

Also classified as Luer/Luer linear connector, single-use.

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

Sources (1)

  • FDA UDI 64c9fe4b-805a-45aa-85b1-4c2a1fc494bd 36 fields · synced May 30, 2026