KaryoMAX® Potassium Chloride Solution

GUDID 10190302001533

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD Cell culture medium IVD

• Primary Device ID: 10190302001533
• NIH Device Record Key: 22eb20bc-90ef-458c-94eb-41add940ea4c
• Commercial Distribution Discontinuation: 2020-04-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: KaryoMAX® Potassium Chloride Solution
• Version Model Number: 10575090
• Company DUNS: 118793157
• Company Name: LIFE TECHNOLOGIES CORPORATION
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10190302001533 [Primary]

FDA Product Code

• KIT: MEDIA AND COMPONENTS, SYNTHETIC CELL AND TISSUE CULTURE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-05-12
• Device Publish Date: 2016-08-01

Devices Manufactured by LIFE TECHNOLOGIES CORPORATION

• 10190302010320 - Human CD138 R-PE Conjugate: 2023-11-30
• 10190302010337 - Human CD138 PE-Cy®5.5 Conjugate: 2023-11-30
• 10190302011730 - Human CD61 APC Conjugate: 2023-11-30
• 10190302000680 - 3500Dx Series Polymer Pouch Caps: 2023-11-20
• 10190302000116 - Histostain® Plus Broad Spectrum: 2023-10-18
• 10190302000123 - invitrogen: 2023-10-18
• 10190302000130 - invitrogen: 2023-10-18
• 10190302008242 - Histostain® Plus 3rd Gen IHC Detection Kit (1000 Slides): 2023-10-18