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Turkel

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Turkel FDA UDI
Generic Name
Aspiration tray, single-use FDA UDI
Device Name
Paracentesis Procedure Tray with Safety Components,8 Fr/Ch x 4-3/4 inch (2.7 mm x 12.1 cm) Catheter FDA UDI
Model / Reference
8888568006 FDA UDI
Description
Paracentesis Procedure Tray with Safety Components,8 Fr/Ch x 4-3/4 inch (2.7 mm x 12.1 cm) Catheter FDA UDI

Identifiers

Catalog Number
8888568006 FDA UDI
Primary DI / UDI-DI
10884521020634 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Aspiration tray, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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
Length — 4.75 Inch FDA UDI
Catheter Gauge — 8 French FDA UDI

Category: Aspiration tray, single-use

Turkel by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aspiration tray, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 9ac02a48-9cb0-4577-9289-4fde30472deb 37 fields · synced May 30, 2026