FIZE kUO Disposable kit Pediatrics

GUDID 07290019239253

FIZE RESEARCH LTD

Urine monitoring system

• Primary Device ID: 07290019239253
• NIH Device Record Key: 5122de2b-517e-4b7c-aac5-8792e2074c1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FIZE kUO Disposable kit Pediatrics
• Version Model Number: FI-FGUS-KU03-0030
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290019239253 [Primary]

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: 2024-03-07
• Device Publish Date: 2024-02-28

On-Brand Devices [FIZE kUO Disposable kit Pediatrics]

• 07290019239253: FI-FGUS-KU03-0030
• 17290019239236: FIZE kUO Disposable kit Pediatrics Catalog Number for 1 Pc: FI-KT00-KU01-0004 FIZE kUO Disposabl