Leica Biosystems RDX QUICKSTOR 8863 USB3

GUDID 00849832013235

Leica Biosystems RDX QUICKSTOR 8863 USB3

Leica Biosystems Richmond, Inc.

Digital storage media

• Primary Device ID: 00849832013235
• NIH Device Record Key: eca92938-c7d8-4d73-ba57-831aa36f1fe4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Leica Biosystems RDX QUICKSTOR 8863 USB3
• Version Model Number: 23RDX8863
• 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: false
• Manufacturing Date: false
• 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	00849832013235 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042542

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: 2
• Public Version Date: 2019-10-07
• Device Publish Date: 2018-06-20

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