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Taut

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
TAUT FDA UDI
Generic Name
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
Device Name
TAUT CHOLANGIOGRAPHY CATHETER 10/BOX 4.5 FRENCH x 30" NO METAL SUPPORT TUBE FDA UDI
Model / Reference
IPN925146 FDA UDI
Description
TAUT CHOLANGIOGRAPHY CATHETER 10/BOX 4.5 FRENCH x 30" NO METAL SUPPORT TUBE FDA UDI

Identifiers

Catalog Number
18305 FDA UDI
Primary DI / UDI-DI
14026704742438 FDA UDI
FDA Product Code
GBZ FDA UDI
GMDN Term
Multi-purpose percutaneous abdominothoracic drainage 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

Yes

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

Category: Multi-purpose percutaneous abdominothoracic drainage catheter

Taut by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose percutaneous abdominothoracic drainage 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 500b9b76-c53f-4e20-97d6-d3054e3d6972 35 fields · synced May 30, 2026