HemaSource

GUDID 10853614008682

Lancet 21G 2.8mm Dual Spring

Hemasource, Inc.

Blood lancet, single-use

• Primary Device ID: 10853614008682
• NIH Device Record Key: 25713038-ef6c-41a0-957a-816510ea7835
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HemaSource
• Version Model Number: BLC2128
• Company DUNS: 009046405
• Company Name: Hemasource, 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853614008685 [Primary]
GS1	10853614008682 [Package]; Contains: 00853614008685; Package: Box [100 Units]; In Commercial Distribution

FDA Product Code

• FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-11-04
• Device Publish Date: 2022-12-08

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