BD Vacutainer®

Basic Information

• Brand Name: BD Vacutainer®
• Primary DI: 50382903650465
• Version / Model: 365046
• Catalog Number: 365046
• Company Name: Becton, Dickinson U.K. Limited
• Labeler DUNS: 225931062
• Distribution Status: Not in Commercial Distribution
• Device Count in Pkg: 1000
• Record Status: Published
• Publish Date: 2016-11-04
• Public Version: 4
• Public Version Date: 2023-04-12
• Public Version Status: Update
• Public Device Record Key: 7888911c-2176-44a6-a700-9e4897e1894c
• Distribution End Date: 2023-03-31

Device Description

BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
JKA	Tubes, vials, systems, serum separators, blood collection	Clinical Chemistry	862.1675	2

GMDN Terms

Code	Name	Definition	Implantable	Status
47587	Evacuated blood collection tube IVD, anticoagulant/separator	A glass or plastic tube, sealed with a stopper, containing a pre-measured amount of vacuum, an anticoagulant [e.g., ethylenediaminetetraacetic acid (EDTA), sodium heparin, sodium citrate, potassium oxalate], and a separator (e.g., gel) to separate blood plasma from cells. It is intended to be used for the collection, and preservation and/or transport, of blood for analysis and/or other investigation (e.g., testing plasma in molecular diagnostics and viral load detection). This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	50382903650465	GS1
Unit of Use	00382903650460	GS1

Premarket Submissions

Submission Number	Supplement Number
K160657	000