CareLiving Blood Lancet 310pcs 83568-1003-14

GUDID 10383568100311

• 30 Gauge • Twist top lancets • Single use • Provides virtually painless testing • Comfort depth penetration • Smooth tri-bevel point • 310 sterile tip lancets per box

Care Living Diagnostics Inc.

Blood lancing device tip

• Primary Device ID: 10383568100311
• NIH Device Record Key: 5edfa055-abfa-45b9-8b4b-d06acfe11bdf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CareLiving Blood Lancet 310pcs
• Version Model Number: LAN30-310
• Catalog Number: 83568-1003-14
• Company DUNS: 125354643
• Company Name: Care Living Diagnostics Inc.
• Device Count: 310
• 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: false
• OTC Over-The-Counter: true

Device Dimensions

• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00383568100314 [Primary]
GS1	10383568100311 [Unit of Use]

FDA Product Code

• QRK: Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

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: 2023-12-04
• Device Publish Date: 2023-11-24

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