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FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
ARROW FDA UDI
Generic Name
Pleural/peritoneal drainage catheterization kit FDA UDI
Device Name
Large Volume Abdominal Paracentesis Kit with Sharps Safety Features FDA UDI
Model / Reference
IPN039807 FDA UDI
Description
Large Volume Abdominal Paracentesis Kit with Sharps Safety Features FDA UDI

Identifiers

Catalog Number
ASK-00376-JHH FDA UDI
Primary DI / UDI-DI
10801902145830 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Pleural/peritoneal drainage catheterization kit 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

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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
Catheter Gauge — 8 French FDA UDI

Category: Pleural/peritoneal drainage catheterization kit

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

Similar devices

Also classified as Pleural/peritoneal drainage catheterization kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI a42b12b0-681a-41e6-b55a-abfbef8687f8 37 fields · synced May 30, 2026