Becton Dickinson and Company, USA 22G x 1 1/4 368608

GUDID 50382903686082

Becton Dickinson and Company, USA 22G x 1 1/4

BECTON, DICKINSON AND COMPANY

Blood collection needle

• Primary Device ID: 50382903686082
• NIH Device Record Key: 5451bd8e-7edc-4628-9b05-d84080768fa5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Becton Dickinson and Company, USA 22G x 1 1/4
• Version Model Number: 368608
• Catalog Number: 368608
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 480
• 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	00382903686087 [Unit of Use]
GS1	50382903686082 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K982541

FDA Product Code

• FMI: Needle, hypodermic, single lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-01-08
• Device Publish Date: 2016-07-28

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• 00382903059065 - BD SafetyGlide: 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 22X1-1/2 RB
• 00382903059096 - BD SafetyGlide: 2025-08-07 SYR 3ML LL W/NDL SFTYGLD 21X1-1/2 RB TW
• 00382903059157 - BD SafetyGlide: 2025-08-07 NEEDLE SFTYGLD 21X1 RB TW
• 00382903059164 - BD SafetyGlide: 2025-08-07 NEEDLE SFTYGLD 25X1 RB
• 00382903059171 - BD SafetyGlide: 2025-08-07 NEEDLE SFTYGLD 21X1-1/2 RB TW
• 00382903059188 - BD SafetyGlide: 2025-08-07 NEEDLE SFTYGLD 18X1-1/2 RB