BD Vacutainer® K2E (EDTA) 7.2mg 368861

GUDID 50382903688611

BD Vacutainer® K2E (EDTA) 7.2mg

Becton, Dickinson U.K. Limited

Evacuated blood collection tube IVD, K2EDTA Evacuated blood collection tube IVD, K2EDTA Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant Evacuated blood collection tube IVD, anticoagulant

• Primary Device ID: 50382903688611
• NIH Device Record Key: 46059f07-785c-4d7f-9590-67c87c8e5ac1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Vacutainer® K2E (EDTA) 7.2mg
• Version Model Number: 368861
• Catalog Number: 368861
• Company DUNS: 225931062
• Company Name: Becton, Dickinson U.K. Limited
• 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	00382903688616 [Unit of Use]
GS1	50382903688611 [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

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