Leica Biosystems Ariol PL220 Automatic Oiler

GUDID 00849832011514

Leica Biosystems Ariol PL220 Automatic Oiler

Leica Biosystems Richmond, Inc.

Cell morphology analyser IVD, automated

• Primary Device ID: 00849832011514
• NIH Device Record Key: 0fec56aa-de6b-4103-b1bc-42e94c49455b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Leica Biosystems Ariol PL220 Automatic Oiler
• Version Model Number: 23ASLSP031
• 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(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com
• Phone: +1(866)4783999
• Email: tech.support@Leicabiosystems.com

Device Dimensions

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• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00849832011514 [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: 2017-03-14

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