Harris Teeter

GUDID 00072036704283

Home Pregnancy Test

Harris Teeter, LLC

Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

• Primary Device ID: 00072036704283
• NIH Device Record Key: 72b826bc-c7fe-491a-a78a-3d6d88b5989e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Harris Teeter
• Version Model Number: 73428
• Company DUNS: 048463103
• Company Name: Harris Teeter, LLC
• Device Count: 2
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00072036704283 [Unit of Use]
GS1	00072036734280 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K984075

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: 2026-03-09
• Device Publish Date: 2026-02-27

On-Brand Devices [Harris Teeter]

• 00072036714299: Home Pregnancy Test
• 00072036704283: Home Pregnancy Test