Leica Biosystems Ariol DM6000 B Basic Configuration Ariol

GUDID 00849832010333

Leica Biosystems Ariol DM6000 B Basic Configuration Ariol

Leica Biosystems Richmond, Inc.

Fluorescence light microscope

• Primary Device ID: 00849832010333
• NIH Device Record Key: b120baf9-7f90-4ace-9570-7fa489a8fd26
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Leica Biosystems Ariol DM6000 B Basic Configuration Ariol
• Version Model Number: 23MIC1201
• 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(866)4783999
• 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	00849832010333 [Primary]

FDA Product Code

• NQN: MICROSCOPE,AUTOMATED,IMAGE ANALYSIS,IMMUNOHISTOCHEMISTRY,OPERATOR INTERVENTION,NUCLEAR INTENSITY & PERCENT POSITIVITY

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: 2016-09-17

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