iFlash-HCG

GUDID 06925912718703

Shenzhen YHLO Biotech Co., Ltd.

Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay

• Primary Device ID: 06925912718703
• NIH Device Record Key: 73b2c0d8-e12a-446f-8f64-818e88ae719f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iFlash-HCG
• Version Model Number: C86012
• Company DUNS: 420735989
• Company Name: Shenzhen YHLO Biotech Co., Ltd.
• 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: false
• Device Combination Product: false
• Single Use: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06925912718703 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223690

FDA Product Code

• DHA: System, Test, Human Chorionic Gonadotropin

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: 2024-02-07
• Device Publish Date: 2024-01-30

Devices Manufactured by Shenzhen YHLO Biotech Co., Ltd.

• 06925912718703 - iFlash-HCG: 2024-02-07
• 06925912718703 - iFlash-HCG: 2024-02-07
• 06925912718833 - iFlash-Anti-Beta2-Glycoprotein I: 2024-01-08 "Beta" is identical to the second letter of Greek alphabet. Because GUDID system couldn't recognize this letter, it is replaced
• 06925912708506 - Reaction vessel: 2022-11-03 2000 pcs/box (2 bag/box, 1000 pcs/bag)
• 06925912710424 - Chemiluminescence Immunoassay Analyzer: 2022-11-03 Type A
• 06925912710462 - Chemiluminescence Immunoassay Analyzer: 2022-11-03 Type B
• 06925912710509 - Chemiluminescence Immunoassay Analyzer: 2022-11-03 Type C
• 06925912710547 - Chemiluminescence Immunoassay Analyzer: 2022-11-03 Type D
• 06925912710578 - Chemiluminescence Immunoassay Analyzer: 2022-11-03