CareLiving Blood Lancet 33G 310pcs Multi-Color 83568-1003-38

GUDID 10383568100335

• 33 Gauge • Multi-Color•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: 10383568100335
• NIH Device Record Key: 5a11d013-68b7-42ca-af1c-f4de1f58552b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CareLiving Blood Lancet 33G 310pcs Multi-Color
• Version Model Number: LAN33-310 Multi-Color
• Catalog Number: 83568-1003-38
• 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: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge
• Needle Gauge: 33 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00383568100338 [Primary]
GS1	10383568100335 [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: 2024-02-02
• Device Publish Date: 2024-01-25

Devices Manufactured by Care Living Diagnostics Inc.

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