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MicroEZ™ IV catheter introducers and guidewires MicroEZ™ Microintroducer

MicroEZ® Microintroducer Kit, A Bevel needle, 50 cm Nitinol Flexura® Guidewire, 6.0 French, 7 cm Length

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1.844.8.BD.LIFE (1.844.823.5433)
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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

Highlights

  • Locking collar
  • Ergonomic handle
  • "Bullet tip" sheath design
  • Funnel design
  • Easy french size identification
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Features and Benefits
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References

Available sizes: 3.5 Fr., 4.5 Fr., 5.0 Fr. & 6.0 Fr.

Please consult product labels, IFU, and package inserts for any indications, contraindications, hazards, warnings, cautions, and instructions for use.

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Specification

GTIN - Case

10801741074704

10

GTIN - each

00801741074707

1


Needle Length

7 cm

Catheter Size

6.0 Fr

Handle Color

Blue

Needle Bevel

A

Guidewire Type

Flexura® guidewire

Length

50 cm

GTIN

GTIN - Case 10801741074704 10
GTIN - each 00801741074707 1

Product Basic Specification

Needle Length 7 cm
Catheter Size 6.0 Fr
Handle Color Blue
Needle Bevel A
Guidewire Type Flexura® guidewire
Length 50 cm
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Electronic Instructions for Use (eIFUs)
Resources
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Frequently Asked Questions
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false
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.
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