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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
Disposable vacuum tubing FDA UDI
Device Name
PATIENT DRAIN TUBE W/ Y-CONNECTOR LATEX FREE FDA UDI
Model / Reference
IPN929928 FDA UDI
Description
PATIENT DRAIN TUBE W/ Y-CONNECTOR LATEX FREE FDA UDI

Identifiers

Catalog Number
S-1120 FDA UDI
Primary DI / UDI-DI
14026704933119 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Disposable vacuum tubing 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

Dimensions & Sizes

Size
Width — 8.7 Inch FDA UDI
Length — 17.9 Inch FDA UDI

Category: Disposable vacuum tubing

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

Similar devices

Also classified as Disposable vacuum tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cddcad60-29f8-4b0f-91b4-b93ba1b28a4e 36 fields · synced May 30, 2026