GUDID 05056080501017

REMEL EUROPE LIMITED

Multiple Brucella species total antibody IVD, kit, agglutination

• Primary Device ID: 05056080501017
• NIH Device Record Key: 1f861d5e-a74e-4790-b76d-6c19f45e6ee2
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: R30164901
• Company DUNS: 232600853
• Company Name: REMEL EUROPE LIMITED
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4401322295600
• Email: ITechnicalSupport@remel.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05056080501017 [Primary]

FDA Product Code

• GSO: Antigens (Febrile), Agglutination, Brucella Spp.

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: 2016-12-09

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