Leica Biosystems CytoVision Removable Archive Device

GUDID 00849832005360

Leica Biosystems CytoVision Removable Archive Device

Leica Biosystems Richmond, Inc.

Digital storage media

• Primary Device ID: 00849832005360
• NIH Device Record Key: a1e893ae-58d1-41a9-8642-72882c0583f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Leica Biosystems CytoVision Removable Archive Device
• Version Model Number: 23RDX
• Company DUNS: 082930884
• Company Name: Leica Biosystems Richmond, 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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: +1(800)5374669
• Email: tech.support@Leicabiosystems.com

Device Dimensions

• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *

Device Identifiers

Device Issuing Agency	Device ID
GS1	00849832005360 [Primary]

FDA Product Code

• JOY: DEVICE, AUTOMATED CELL-LOCATING

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-10-07
• Device Publish Date: 2016-09-17

On-Brand Devices [Leica Biosystems CytoVision Removable Archive Device]

• 00849832005360: Leica Biosystems CytoVision Removable Archive Device
• 00849832005155: Leica Biosystems Cytovision Removable Archive Device