PrecisionGlide 303302

GUDID 50382903033022

NEEDLE 27X3/8 IB

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use

• Primary Device ID: 50382903033022
• NIH Device Record Key: fa07d8a6-72a2-4cbb-98e7-a5b15e9a0aff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PrecisionGlide
• Version Model Number: 303302
• Catalog Number: 303302
• 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

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
• 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	00382903033027 [Primary]
GS1	30382903033028 [Package]; Contains: 00382903033027; Package: Shelfpack [100 Units]; In Commercial Distribution
GS1	50382903033022 [Package]; Contains: 30382903033028; Package: Case [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021475

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: 2023-09-11
• Device Publish Date: 2023-09-02

Devices Manufactured by BECTON, DICKINSON AND COMPANY

• 00382903059041 - BD SafetyGlide: 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 25X5/8 RB
• 00382903059058 - BD SafetyGlide: 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 23X1 RB
• 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