{"AlternateComparison":false,"RelatedProducts":false,"Specification":true,"FeatureBenefit":false}
BD Twinpak™ IV accessories BD® Blunt Plastic Cannulas and Accessories

BD Twinpak™ Dual Cannula Device with 3 mL Syringe

Icon to close the modal
Support
Sales
Phone Icon
1.844.8.BD.LIFE (1.844.823.5433)
Modal Close Icon

Capability:

Product Line:

Icon to close thank you modal
Thank you for contacting our sales team!
A sales representative will get in touch with you shortly.
Ordering
Phone Icon
1.800.482.4822
6 a.m. to 3 p.m. PT Monday to Friday
Fax Icon
1.800.447.7825
CustCareInfusion@carefusion.com
Customer Service
Phone Icon
1.866.488.1408
6am-5pm PST Monday to Friday
DL-US-INF-Tech-Support@bd.com
Overview

BD® Blunt Plastic Cannula are specifically designed for use with preslit injection sites and vials designed for needleless access. They are not compatible with conventional injection sites that are not preslit. The BD® Blunt Plastic Cannula is intended for use with Abbott LifeShield®, McGaw SafeLine™ and Baxter InterLink® Systems.

The BD Twinpak™ Dual Cannula Device contains the components you need for syringe filling and needleless delivery of syringe contents into a preslit injection site. The BD Twinpak™  Dual Cannula Device contains an opaque red hub syringe filling device for syringe filling from vials or ampoules and a BD® Blunt Plastic Cannula for safe IV fluid delivery or aspiration through preslit injection sites. The red hub syringe filling device is not intended for accessing injection sites or for percutaneous injections.

BD® Vial Access Cannula are specifically designed for use with the Interlink® injection sites, identified by a colored alert ring around the septum.

true
Features and Benefits
Promotional Story
false
References
false
Specification

GTIN - Case

50382903033916

800

GTIN - Shelfpack

30382903033912

100

GTIN - each

00382903033911

1


DEHP is not part of the Material Formulation

Yes

Natural Latex

Yes


CE Marking

No

Country of Manufacture

United States


Case Dimensions

21.7 in x 15.6 in x 15.6 in

Quantity

800

Unit of Measure

Per Case


Color of Tubing

None

Filter

None

Manifold

None

Number of Backcheck Valves

0

Number of Connectors

0

Number of Fuses

0

Number of Y-Sites

0

Sterility

Content sterile

Stopcock

None

T-Connector Type

None

Type of Connector

None

Weight

17.3 lb

Y-Site Port Type

None

GTIN

GTIN - Case 50382903033916 800
GTIN - Shelfpack 30382903033912 100
GTIN - each 00382903033911 1

FDA, Premarket Approval, and Regulatory

DEHP is not part of the Material Formulation Yes
Natural Latex Yes

Manufacturing

CE Marking No
Country of Manufacture United States

Packaging

Case Dimensions 21.7 in x 15.6 in x 15.6 in
Quantity 800
Unit of Measure Per Case

Product Basic Specification

Color of Tubing None
Filter None
Manifold None
Number of Backcheck Valves 0
Number of Connectors 0
Number of Fuses 0
Number of Y-Sites 0
Sterility Content sterile
Stopcock None
T-Connector Type None
Type of Connector None
Weight 17.3 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
Literature Icon
Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
References
false
false