FIRSTVIEW Luteinizing Hormone Rapid Test Strip LH-1011

GUDID 06974246462400

Safecare Biotech (Hangzhou) Co., Ltd.

Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing

• Primary Device ID: 06974246462400
• NIH Device Record Key: 632b01a4-c303-4be5-b687-4ddf42654378
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FIRSTVIEW Luteinizing Hormone Rapid Test Strip
• Version Model Number: 35 tests
• Catalog Number: LH-1011
• Company DUNS: 544349634
• Company Name: Safecare Biotech (Hangzhou) Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	06974246462400 [Primary]

FDA Product Code

• NGE: Test, Luteinizing Hormone (Lh), 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: 2025-08-07
• Device Publish Date: 2025-07-30

On-Brand Devices [FIRSTVIEW Luteinizing Hormone Rapid Test Strip]

• 06974246460864: LH-1011
• 06974246460871: LH-1011
• 06974246462417: 15 tests
• 06974246462400: 35 tests