Stem-Kit Reagents IM3630

GUDID 15099590220006

Stem-Kit Reagents

Beckman Coulter, Inc.

Fixative, Orth's solution

• Primary Device ID: 15099590220006
• NIH Device Record Key: 2a16e4a6-9995-41bf-819e-0b98d38df039
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Stem-Kit Reagents
• Version Model Number: IM3630
• Catalog Number: IM3630
• Company DUNS: 008254708
• Company Name: Beckman Coulter, 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	15099590220006 [Primary]

FDA Product Code

• GKZ: Counter, Differential Cell

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: 2016-09-23

On-Brand Devices [Stem-Kit Reagents]

• 15099590220006: Stem-Kit Reagents
• 15099590762889: Stem-Kit Reagents