URINARY TRACT INFECTION TEST UTI-1021

GUDID 06974246461359

Safecare Biotech (Hangzhou) Co., Ltd.

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• Primary Device ID: 06974246461359
• NIH Device Record Key: ca06f3a0-8d96-427f-91bb-a111a9eddc1b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: URINARY TRACT INFECTION TEST
• Version Model Number: 5 tests
• Catalog Number: UTI-1021
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974246461359 [Primary]

FDA Product Code

• LJX: Test, Urine Leukocyte

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: 2024-05-20
• Device Publish Date: 2024-05-11

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• 06974246461342 - Vaginal PH Rapid Test Cassette: 2024-05-20
• 06974246461359 - URINARY TRACT INFECTION TEST: 2024-05-20
• 06974246461359 - URINARY TRACT INFECTION TEST: 2024-05-20
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