BD Vacutainer® K2 EDTA 7.2mg 368021

GUDID 50382903680219

BD Vacutainer® K2 EDTA 7.2mg

BECTON, DICKINSON AND COMPANY

Evacuated blood collection tube IVD, K2EDTA

• Primary Device ID: 50382903680219
• NIH Device Record Key: d20e0f49-3cc2-4f64-a1ef-d1d5d369ca48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Vacutainer® K2 EDTA 7.2mg
• Version Model Number: 368021
• Catalog Number: 368021
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 1000
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903680214 [Unit of Use]
GS1	50382903680219 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK050036

FDA Product Code

• JKA: Tubes, vials, systems, serum separators, blood collection

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-07-28

On-Brand Devices [BD Vacutainer® K2 EDTA 7.2mg]

• 50382903680219: BD Vacutainer® K2 EDTA 7.2mg
• 50382903678612: BD Vacutainer® K2 EDTA 7.2mg
• 50382903678445: BD Vacutainer® K2 EDTA 7.2mg
• 30382903678618: BD Vacutainer® K2 EDTA 7.2mg