Pipettor Module W086-090

GUDID 58050148218277

Pipettor Module

COPAN WASP SRL

Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD Microbial specimen inoculation/streaking/colony-picking instrument IVD

• Primary Device ID: 58050148218277
• NIH Device Record Key: 39bc38c6-146d-40d6-ba92-ea1a6df3edef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pipettor Module
• Version Model Number: W086-090
• Catalog Number: W086-090
• Company DUNS: 434263590
• Company Name: COPAN WASP SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com
• Phone: +390302687218
• Email: wasp@copangroup.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	58050148218277 [Primary]

FDA Product Code

• JTC: Device, Microtiter Diluting/Dispensing

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-05
• Device Publish Date: 2021-04-27

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• 58059796361700 - URIVerse™: 2023-10-30 URIVerse™
• 08050148218005 - Colibri Daily Verification Kit: 2022-11-23 Colibri Daily Verification Kit
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• 18050148217968 - Colibrí™ Primary Tube for VITEK 2: 2022-11-23 Colibrí™ Primary Tube for VITEK 2
• 58050148218208 - Colibrí™: 2022-11-23 Colibrí™
• 58052870818923 - External Loader - Turn Table: 2022-06-03 External Loader - Turn Table