Lia Pregnancy Test

GUDID 00860000380621

Lia Diagnostics, Inc.

Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, agglutination, rapid

• Primary Device ID: 00860000380621
• NIH Device Record Key: a7c3f897-3ae0-482b-876b-8c61845ba4fb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lia Pregnancy Test
• Version Model Number: 2 Pack
• Company DUNS: 079828691
• Company Name: Lia 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: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860000380621 [Primary]

FDA Product Code

• LCX: Kit, Test, Pregnancy, Hcg, Over The Counter

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-23
• Device Publish Date: 2021-03-15

On-Brand Devices [Lia Pregnancy Test]

• 00860000380621: 2 Pack
• 00860000380607: 2 Pack Discreet