Rite Aid

GUDID 30011822024410

Rite Aid Pregnancy Tests, 1 Digital Pregnancy Rapid Test + 1 Early Detection Pregnancy Test, combo test kit

Guangzhou Decheng Biotechnology Co., LTD

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

• Primary Device ID: 30011822024410
• NIH Device Record Key: 8dfa2a40-f81e-4e3c-a8ce-ad0e05ef62a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rite Aid
• Version Model Number: 2T
• Company DUNS: 554534314
• Company Name: Guangzhou Decheng Biotechnology Co., LTD
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	00011822024419 [Primary]
GS1	30011822024410 [Unit of Use]

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: 2024-10-07
• Device Publish Date: 2024-09-27

On-Brand Devices [Rite Aid]

• 30011822024427: Rite Aid Pregnancy Tests, 1 Digital Pregnancy Rapid Test + 1 Pregnancy Rapid Test Midstream, com
• 30011822024410: Rite Aid Pregnancy Tests, 1 Digital Pregnancy Rapid Test + 1 Early Detection Pregnancy Test, com