EZCHECK

GUDID 30850065976595

EZCHECK® Multi-Drug Urine Test Dipcard, 6-Panel, 5T/Box

Guangzhou Decheng Biotechnology Co., LTD

Tricyclic antidepressant IVD, kit, rapid ICT, clinical

• Primary Device ID: 30850065976595
• NIH Device Record Key: 637c9d29-7d73-46b8-8716-1138ab02ff6d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EZCHECK
• Version Model Number: EZDOA-264
• Company DUNS: 554534314
• Company Name: Guangzhou Decheng Biotechnology Co., LTD
• Device Count: 5
• 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	00850065976594 [Primary]
GS1	30850065976595 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240698

FDA Product Code

• PTG: Test, Methadone, 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 [EZCHECK]

• 30850065976601: EZCHECK® Multi-Drug Urine Test Clicker Cup, 14-Panel, 25T/Box
• 30850065976595: EZCHECK® Multi-Drug Urine Test Dipcard, 6-Panel, 5T/Box