FIZE kUO Disposable Kit FI-KT00-KU01-0007

GUDID 17290019239212

FIZE kUO Disposable Kit catalog number for 1 pc: FI-KT00-KU01-0007 FIZE kUO Disposable Kit catalog number for 10 pcs: FI-FG00-KU03-0003

FIZE RESEARCH LTD

Urine monitoring system

• Primary Device ID: 17290019239212
• NIH Device Record Key: d2b6e5f5-882e-43e0-a6ed-8f4018006347
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FIZE kUO Disposable Kit
• Version Model Number: G2
• Catalog Number: FI-KT00-KU01-0007
• Company DUNS: 649273943
• Company Name: FIZE RESEARCH LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290019239215 [Primary]
GS1	17290019239212 [Package]; Contains: 07290019239215; Package: BOX [10 Units]; In Commercial Distribution

FDA Product Code

• EXY: Uroflowmeter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-07
• Device Publish Date: 2025-04-29

On-Brand Devices [FIZE kUO Disposable Kit ]

• 17290019239243: FIZE kUO Disposable Kit Catalog number for 1 pc: FI-KT00-KU01-0001 Catalog number for 10 pcs in
• 17290019239212: FIZE kUO Disposable Kit catalog number for 1 pc: FI-KT00-KU01-0007 FIZE kUO Disposable Kit catal