CareLiving Safety Lancet 30

GUDID 00383568100222

Safety lancet 30G*1.8mm,100 Sterile Tip Lancets Per Box,One Handed Use,No Lancing Device Required,Automic Needle Retraction,Lock out after use is a Safety Feature That Negates Needle stick injuries And Prevents Blood cross-contamination

Care Living Diagnostics Inc.

Manual blood lancing device, single-use

• Primary Device ID: 00383568100222
• NIH Device Record Key: ca2c9eef-86fb-47b0-8656-a4df555cb5d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CareLiving Safety Lancet 30
• Version Model Number: Safety Lancet 30
• Company DUNS: 125354643
• Company Name: Care Living Diagnostics Inc.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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
• Needle Gauge: 30 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00383568100222 [Primary]
GS1	10383568100229 [Package]; Package: [50 Units]; Discontinued: 2023-11-17; Not in Commercial Distribution

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: 2023-11-23
• Device Publish Date: 2023-11-15

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