BD Blunt Filter NRFit 400066

GUDID 30382904000661

BD® Blunt Filter NRFit™ Needle, 18G x 1 1/2 in

BECTON, DICKINSON AND COMPANY

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• Primary Device ID: 30382904000661
• NIH Device Record Key: 049023c2-9c76-4c7a-b7df-ce48b3733f6b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Blunt Filter NRFit
• Version Model Number: 400066
• Catalog Number: 400066
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382904000660 [Primary]
GS1	30382904000661 [Package]; Contains: 00382904000660; Package: Shelfpack [80 Units]; In Commercial Distribution
GS1	50382904000665 [Package]; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• GAA: NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

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: 2022-08-09
• Device Publish Date: 2022-08-01

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