BD Eclipse™ Needle with SmartSlip™ Technology 302436

GUDID 00382903024360

NEEDLE 27X1-1/2 ECLIPSE

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use

• Primary Device ID: 00382903024360
• NIH Device Record Key: e71903dc-dc1a-41c8-a1ae-1b953ca75be9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Eclipse™ Needle with SmartSlip™ Technology
• Version Model Number: 302436
• Catalog Number: 302436
• 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: 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
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903024360 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100209

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: 2
• Public Version Date: 2025-07-31
• Device Publish Date: 2020-09-25

On-Brand Devices [BD Eclipse™ Needle with SmartSlip™ Technology]

• 30382903058991: NEEDLE ECLIPSE S/T 20X1 RB
• 30382903058946: NEEDLE ECLIPSE S/T 21X1 RB TW
• 30382903058915: NEEDLE ECLIPSE S/T 25X1 RB
• 30382903058892: NEEDLE ECLIPSE S/T 27X3/4 RB
• 30382903058885: NEEDLE ECLIPSE S/T 20X1-1/2 RB
• 30382903058861: NEEDLE 23X1-1/4 ECLIPSE SMARTSLIP
• 30382903057604: NEEDLE ECLIPSE S/T 25X5/8 RB
• 30382903024361: NEEDLE 27X1-1/2 ECLIPSE
• 00382903024360: NEEDLE 27X1-1/2 ECLIPSE