CDS™ 3-PD Hematology Control 502-004

GUDID 00812137010247

For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments. CDS 3PD Hematology Control is prepared from stabilized human blood so that repeated measurements can be made daily to monitor the performance of hematology analyzer systems. ASSIGNED VALUES and EXPECTED RANGES are determined on systems using specific CDS reagents. ASSIGNED VALUES are confirmed by multiple analysis of the control product and should be considered a suggested average until you establish your own running mean.

CLINICAL DIAGNOSTIC SOLUTIONS, INC.

Full blood count IVD, control Full blood count IVD, control

• Primary Device ID: 00812137010247
• NIH Device Record Key: ff43c6d9-ed4c-48d1-ab73-0ce2f5614eb8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CDS™ 3-PD Hematology Control
• Version Model Number: Tri-Pack 6x3.0mL
• Catalog Number: 502-004
• Company DUNS: 048144997
• Company Name: CLINICAL DIAGNOSTIC SOLUTIONS, INC.
• Device Count: 6
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8004533328
• Email: quality@cdsolinc.com
• Phone: 8004533328
• Email: quality@cdsolinc.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 10 Degrees Celsius
• Storage Environment Temperature: Between 2 Degrees Celsius and 10 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812137010247 [Primary]
GS1	00812137011770 [Unit of Use]

FDA Product Code

• JPK: Mixture, Hematology Quality Control

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-02

Devices Manufactured by CLINICAL DIAGNOSTIC SOLUTIONS, INC.

• 00001812701208 - Triglycerides Reagent: 2020-03-31 For the in vitro quantitative determination of Triglycerides in serum or plasma. Triglycerides determinations are of interest in
• 00812137011848 - Albumin Reagent: 2020-03-31 For the quantitative determination of Albumin in serum.
• 00812137010254 - CDS-LTX CONTROL: 2018-07-06 CDS-LTX Control is used to validate volume, conductivity and light scatter parameters on COULTER HmX/ MAXM, STKS and GEN-S in
• 00812137010261 - CDS-LTX PRIMER: 2018-07-06 CDS-LTX Primer is used to prepare the tubing and instrument components on the COULTER HmX/MAXM, STKS and GEN-S instruments pr
• 00812137011947 - Carbon Dioxide Reagent: 2018-06-11 For the quantitative determination of Carbon Dioxide in serum. For in vitro diagnostic use only.
• 00812137011916 - Urea Nitrogen Reagent Set: 2018-04-17 For the quantitative determination of urea nitrogen in serum. For in vitro diagnostic use only. Determination of urea nitrogen
• 00081213701184 - Albumin Reagent: 2018-03-29 For the quantitative determination of Albumin in serum.
• 00812137010216 - Boule Con-Diff Tri-Level: 2018-03-29 For in vitro diagnostic use as a control to monitor the performance of multi- parameter hematology instruments. Boule Con-Diff T