Eclipse Needle 303278

GUDID 50382903032780

NEEDLE ECLIPSE 23X1-1/2 RB TW BNS

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use

• Primary Device ID: 50382903032780
• NIH Device Record Key: be63c267-33eb-4a64-9e1b-ab8822e4c36e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Eclipse Needle
• Version Model Number: 303278
• Catalog Number: 303278
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 1
• 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	00382903032785 [Primary]
GS1	50382903032780 [Package]; Contains: 00382903032785; Package: Case [6000 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161170

FDA Product Code

• FMI: Needle, hypodermic, single lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-21
• Device Publish Date: 2024-11-13

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