URIC ACID (UA)

GUDID 05055273209563

RANDOX LABORATORIES LIMITED

Uric acid IVD, kit, enzyme spectrophotometry

• Primary Device ID: 05055273209563
• NIH Device Record Key: 60941631-3d81-4c42-8be9-953418b3811c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: URIC ACID (UA)
• Version Model Number: UA8069
• Company DUNS: 227530649
• Company Name: RANDOX LABORATORIES LIMITED
• 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: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055273209563 [Primary]

FDA Product Code

• KNK: Acid, Uric, Uricase (Colorimetric)

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: 2019-06-11
• Device Publish Date: 2019-06-03

On-Brand Devices [URIC ACID (UA)]

• 05055273209570: UA8333
• 05055273209563: UA8069
• 05055273206753: UA7972
• 05055273206746: For the quantitative in vitro determination of Uric Acid in serum, plasma and urine.
• 05055273206739: For the quantitative in vitro determination of Uric Acid in serum, plasma and urine.
• 05055273206708: For the quantitative in vitro determination of Uric Acid in serum, plasma and urine.