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MiniLoc™ Port access devices MiniLoc™ Safety Infusion Set

MiniLoc™ Safety Infusion Set with Y-Injection Site and Medegen® Needleless Injection Cap, 20 G x 0.50 in.

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1.844.8.BD.LIFE (1.844.823.5433)
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BD® Port Access Kits and Needles

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Customer Service
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1.844.8.BD.LIFE (1.844.823.5433)
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1.800.847.2220
OEM@bd.com
Overview

The safety mechanism on the MiniLoc™ Safety Infusion Set is an easy to use, single step safety activation. The needle point safety is designed to help reduce the risk of needlestick injuries.

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Features and Benefits
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Specification

GTIN - Each

00801741048951

1

GTIN - Shelfpack

10801741048958

20

GTIN - Case

20801741048955

160


Minimum Order Quantity

1 shelfpack

Package

20/shelfpack


Size

20 Ga

Length

0.50"

Y-Site

with Y-Injection Site and Medegen™ Needleless Injection Cap

GTIN

GTIN - Each 00801741048951 1
GTIN - Shelfpack 10801741048958 20
GTIN - Case 20801741048955 160

Packaging

Minimum Order Quantity 1 shelfpack
Package 20/shelfpack

Product Basic Specification

Size 20 Ga
Length 0.50"
Y-Site with Y-Injection Site and Medegen™ Needleless Injection Cap
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Electronic Instructions for Use (eIFUs)
Resources
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Frequently Asked Questions
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Related Products
RELATED PRODUCTS NOT AVAILABLE
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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
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Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
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