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Texium™ Texium™ closed male luer

SKU:

10012241-0500

GTIN:

10885403221705

Texium^™ closed male luer with female cap, 0.12 mL

Overview
Specifications
eIFUs and Resources
Product Notifications

Our Texium™ closed male luer partners with our SmartSite™ needle-free valve products to form a closed system that keeps hazardous drugs from leaking or dripping.

GTIN - Shelfpack

20885403221702

GTIN - each

10885403221705

GTIN - Case

50885403221703

FDA, Premarket Approval, and Regulatory

Natural Latex

Registered with Health Canada

Manufacturing

CE Marking

Packaging

Case Dimensions

8.375 in x 7.375 in x 6.625 in 1.2 lb

Product Basic Specification

Approximate Priming Volume

0.12 mL

Color of Tubing

Filter

Luer Lock Type

Texium™ Closed Male Luer

Manifold

Number of Backcheck Valves

Number of Connectors

Number of Fuses

Number of Y-Sites

Sterility

Fluid Path Sterile

Stopcock

T-Connector Type

Texium™

Type of Connector

Texium™

Weight

1.2 lb

Y-Site Port Type

GTIN

GTIN - Shelfpack	20885403221702	50
GTIN - each	10885403221705	1
GTIN - Case	50885403221703	100

FDA, Premarket Approval, and Regulatory

Natural Latex	Yes
Registered with Health Canada	Yes

Manufacturing

CE Marking

Packaging

Case Dimensions

8.375 in x 7.375 in x 6.625 in 1.2 lb

Product Basic Specification

Approximate Priming Volume	0.12 mL
Color of Tubing	None
Filter	None
Luer Lock Type	Texium™ Closed Male Luer
Manifold	None
Number of Backcheck Valves	0
Number of Connectors	0
Number of Fuses	0
Number of Y-Sites	0
Sterility	Fluid Path Sterile
Stopcock	None
T-Connector Type	None
Texium™	Yes
Type of Connector	Texium™
Weight	1.2 lb
Y-Site Port Type	None

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North American Regional Complaint Center

1-844-8BD-LIFE (1-844-823-5433)

productcomplaints@bd.com

Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:

Product Name and/or Catalog Number
Lot Number or Serial Number
Any injuries and/or Harm?
What is the issue you experienced?
Is the actual sample or sample representative available? (If possible, please send affected sample)
Contact name and phone number

These recall notices provide current information on medical device recalls.

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