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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
General-purpose catheter connector, sterile FDA UDI
Device Name
PE SAHARA DRY SUCT/DRY SEAL LF FDA UDI
Model / Reference
IPN025424 FDA UDI
Description
PE SAHARA DRY SUCT/DRY SEAL LF FDA UDI

Identifiers

Catalog Number
S-1100-08LF FDA UDI
Primary DI / UDI-DI
34026704428909 FDA UDI
510(k) Number
K962856 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
General-purpose catheter connector, sterile 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

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
Length — 10.5 Inch FDA UDI
Total Volume — 2000 Milliliter FDA UDI
Depth — 3.5 Inch FDA UDI
Width — 11.25 Inch FDA UDI

Category: General-purpose catheter connector, sterile

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

Similar devices

Also classified as General-purpose catheter connector, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 61469314-8877-4ca9-8959-0cac08c6e85a 37 fields · synced Jun 1, 2026