BD SafetyGlide 23x1-1/2 RB TW 304387

GUDID 50382903043878

NEEDLE SAFETYGLIDE 23X1-1/2 RB TW

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use

• Primary Device ID: 50382903043878
• NIH Device Record Key: 9bbe7222-4974-47be-8f1e-6e97df197737
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD SafetyGlide 23x1-1/2 RB TW
• Version Model Number: 304387
• Catalog Number: 304387
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 50
• 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: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge
• Length: 1.5 Inch
• Needle Gauge: 23 Gauge

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	00382903043873 [Unit of Use]
GS1	30382903043874 [Primary]
GS1	50382903043878 [Package]; Contains: 30382903043874; Package: Case [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K951254

FDA Product Code

• FMI: Needle, hypodermic, single lumen

Sterilization

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

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

[50382903043878]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-09
• Device Publish Date: 2023-08-01

Devices Manufactured by BECTON, DICKINSON AND COMPANY

• 00382904413576 - BD ProbeTec™ Qx Collection Kit for Endocervical or Lesion Specimens: 2025-08-25 BD ProbeTec™ Qx Collection Kit for Endocervical or Lesion Specimens Contains: 100 each sterile polyester-tipped cleaning swab,
• 00382904413583 - Male Urethral Collection Kit for BD ProbeTec™ (CT/GC) Qx Amplified DNA Assays: 2025-08-25 Swab Male Urethral Specimen Collection
• 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