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Texium™ closed male luer with female cap, 0.12 mL

Overview
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Features and Benefits
Promotional Story
false
References
false
Specification

GTIN - Shelfpack

20885403221702

50

GTIN - each

10885403221705

1

GTIN - Case

50885403221703

100


Natural Latex

Yes

Registered with Health Canada

Yes


CE Marking

No


Case Dimensions

8.375 in x 7.375 in x 6.625 in 1.2 lb


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

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 No

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
References
false
Electronic Instructions for Use (eIFUs)
Resources
References
false
Frequently Asked Questions
false
References
false
Related Products
RELATED PRODUCTS NOT AVAILABLE
References
false
Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
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
Product Recalls
Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
References
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false