Turkel 566034

GUDID 20884521020594

Multi-purpose percutaneous abdominothoracic drainage catheter

Primary Device ID	20884521020594
NIH Device Record Key	5e402faf-ac83-49c5-8404-aca8c9fcb69c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Turkel
Version Model Number	566034
Catalog Number	566034
Company DUNS	080935429
Company Name	Cardinal Health, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	true

Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;

Device Issuing Agency	Device ID
GS1	10884521020597 [Primary]
GS1	20884521020594 [Package] Contains: 10884521020597 Package: PACK_OR_INNER_PACK [20 Units] In Commercial Distribution
GS1	30884521020591 [Package] Contains: 10884521020597 Package: CASE [160 Units] In Commercial Distribution

GAA	NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

Steralize Prior To Use	false
Device Is Sterile	true

20884521020594	Safety Fluid Drainage System
20884521020631	Paracentesis Procedure Tray with Safety Components,8 Fr/Ch x 4-3/4 inch (2.7 mm x 12.1 cm) Cathe
20884521020617	Safety Thoracentesis Procedural Tray,8 Fr/Ch (2.7 mm) x 5"" (12.7 cm) Catheter
20884521020600	Safety Thoracentesis Procedural Tray,8 Fr/Ch (2.7mm) x 3-1/2"" (8.9 cm) Catheter

Mark Image Registration \| Serial	Company Trademark Application Date
TURKEL 78832966 3348305 Live/Registered	CARDINAL HEALTH 529, LLC 2006-03-09
TURKEL 74429836 not registered Dead/Abandoned	SYMBIOSIS CORPORATION 1993-08-30
TURKEL 74361207 1846177 Dead/Cancelled	SYMBIOSIS CORPORATION 1993-02-22