Calcium (Ca) CA2390

GUDID 05055273200881

The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine

RANDOX LABORATORIES LIMITED

Calcium (Ca2+) IVD, reagent

• Primary Device ID: 05055273200881
• NIH Device Record Key: ffe52b6d-458d-40bd-b9f2-c551a97c678c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Calcium (Ca)
• Version Model Number: CA2390
• Catalog Number: CA2390
• Company DUNS: 227530649
• Company Name: RANDOX LABORATORIES LIMITED
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +442894451070
• Email: technical.services@randox.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 15 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055273200881 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K974607

FDA Product Code

• CJY: Azo Dye, Calcium

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-16

On-Brand Devices [Calcium (Ca)]

• 05055273200881: The calcium test system is a device intended for the quantitative in vitro determination of calc
• 05055273208368: CA8309