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StatLock™ StatLock™ Arterial Plus Stabilization Device

StatLock™ Arterial Plus Stabilization Device - Crescent Tricot

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1.844.8.BD.LIFE (1.844.823.5433)
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StatLock™ Stabilization Devices

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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 color-coded red retainer, designed for patient safety, is the most sophisticated StatLock® Stabilization Device retainer ever.
  • Unique entry angle of retainer is designed to prevent catheter kinking, which could lead to occlusion.
  • The precision molded, ergonomic retainer can be opened and closed while in place, allowing for tubeset changes whenever necessary.
  • The StatLock® Arterial Plus Stabilization Device fits adult and pediatric (over 18 months) patients.
  • Breathable anchor pad made from nonabsorbent tricot polyester.
  • Sterile, DEHP-free and latex-free.
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Features and Benefits
FEATURE AND BENEFIT CARDS NOT AVAILABLE
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References

Specifications subject to change without notice.

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 - Box

20801741081280

250

GTIN - Each

00801741081286

1

GTIN - Case

10801741081283

25

Natural Latex

No

Quantity

25/case

Stand Alone or Kit

Stand Alone

GTIN

GTIN - Box 20801741081280 250
GTIN - Each 00801741081286 1
GTIN - Case 10801741081283 25

FDA, Premarket Approval, and Regulatory

Natural Latex No

Packaging

Quantity 25/case
Stand Alone or Kit Stand Alone
References
false
Electronic Instructions for Use (eIFUs)
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Frequently Asked Questions
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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
productcomplaints@bd.com
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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These recall notices provide current information on medical device recalls.
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