BUN/BS200 BUN600

GUDID 00817439020307

For the quantitative determination of urea nitrogen in serum using the Mindray BS-200 analyzer. For in vitro diagnostic use only. 3 x 40ml, 3 x 10ml

Medtest Dx, Inc.

Urea IVD, kit, enzyme spectrophotometry

• Primary Device ID: 00817439020307
• NIH Device Record Key: 46c88bea-36cd-43df-bf9a-6bd904a2eafd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BUN/BS200
• Version Model Number: BUN600
• Catalog Number: BUN600
• Company DUNS: 070371210
• Company Name: Medtest Dx, Inc.
• 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: false
• 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: 800-445-9853
• Email: techservice@medtest.com
• Phone: 800-445-9853
• Email: techservice@medtest.com
• Phone: 800-445-9853
• Email: techservice@medtest.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817439020307 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972671

FDA Product Code

• CDQ: Urease And Glutamic Dehydrogenase, Urea Nitrogen

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: 2016-09-27

Devices Manufactured by Medtest Dx, Inc.

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• 00817439020024 - Direct Lipid Control L2: 2018-07-06 This product is intended for in-vitro use only, in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), and Apolipopr
• 00817439020031 - Direct Lipid Control L3: 2018-07-06 This product is intended for in-vitro use only, in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), and Apolipopr
• 00817439020093 - Albumin / BS480: 2018-07-06 For the quantitative determination of Albumin in serum using the Mindray BS-480 analyzer. In vitro diagnostic medical device. 8
• 00817439020109 - Albumin: 2018-07-06 For the quantitative in vitro determination of Albumin in serum and plasma on the Polychem 180 analyzer. 9 x 51 ml
• 00817439020116 - Albumin / BS200: 2018-07-06 For the quantitative determination of Albumin in serum using the Mindray BS-200 analyzer. 4 x 40 ml
• 00817439020123 - Alkaline Phos/ BS480: 2018-07-06 For the quantitative determination of Albumin in serum using the Mindray BS-480 analyzer. In vitro diagnostic medical device.
• 00817439020130 - ALP Reagent: 2018-07-06 For the quantitative in vitro determination of Alkaline Phosphatase (ALP) in serum and plasma. 6 x 51 ml, 6 x 14 ml