20G 1 1/4IN sterile Spinal Introducer needle 405160

GUDID 00382904051600

NEEDLE SP S/SU 20GA 1-1/4IN INTRODUCER

BECTON, DICKINSON AND COMPANY

Needle guide, single-use

• Primary Device ID: 00382904051600
• NIH Device Record Key: 042946e6-1d98-4d07-8fc6-bf62c35ef21e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 20G 1 1/4IN sterile Spinal Introducer needle
• Version Model Number: 405160
• Catalog Number: 405160
• 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 Dimensions

• Length: 1.25 Inch
• Length: 1.25 Inch
• Length: 1.25 Inch
• Length: 1.25 Inch
• Length: 1.25 Inch
• Length: 1.25 Inch
• Length: 1.25 Inch
• Length: 1.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382904051600 [Primary]
GS1	30382904051601 [Package]; Package: Shelfpack [25 Units]; In Commercial Distribution
GS1	50382904051605 [Package]; Contains: 30382904051601; Package: Case [4 Units]; In Commercial Distribution

FDA Product Code

• BSP: NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 11
• Public Version Date: 2026-02-06
• Device Publish Date: 2016-09-16

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