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BD Aptra™ Cystoscopes

BD Aptra™ Single-Use Digital Flexible Cystoscope Reverse Deflection Model

The reverse deflection model of the BD Aptra™ Single-Use Digital Flexible Cystoscope is a sterile, single-use device comprised of two main components: a control body with articulation controls, accessory access ports and cable; and a flexible insertion tube. The flexible insertion tube is the applied part composed by a rigid distal tip, deflection section and shaft.

Overview
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Features and Benefits
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Specification

GTIN - Box

20850023925392

20

GTIN - Each

00850023925398

1

GTIN - Case

10850023925395

2


Field of view

100 degrees

Depth of field

2-50 mm

Distal tip diameter

9 Fr

Insertion tube outer diameter

13.8 Fr

Working Channel Diameter

6.6 Fr

Angulation range

210' Up / 210' Down

GTIN

GTIN - Box 20850023925392 20
GTIN - Each 00850023925398 1
GTIN - Case 10850023925395 2

Product Basic Specification

Field of view 100 degrees
Depth of field 2-50 mm
Distal tip diameter 9 Fr
Insertion tube outer diameter 13.8 Fr
Working Channel Diameter 6.6 Fr
Angulation range 210' Up / 210' Down
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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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