Proteus OXK Agglutinating Serum

GUDID 05056080501611

REMEL EUROPE LIMITED

Multiple Rickettsia species (spotted fever group) total antibody IVD, control Multiple Rickettsia species (spotted fever group) total antibody IVD, control Multiple Rickettsia species (spotted fever group) total antibody IVD, control Multiple Rickettsia species (spotted fever group) total antibody IVD, control Multiple Rickettsia species (spotted fever group) total antibody IVD, control Multiple Rickettsia species (spotted fever group) total antibody IVD, control Multiple Rickettsia species (spotted fever group) total antibody IVD, control

• Primary Device ID: 05056080501611
• NIH Device Record Key: 62f0a181-4dbd-4b5a-a948-4feb8843e17a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Proteus OXK Agglutinating Serum
• Version Model Number: R30165901
• 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: +4401256694238
• Email: microbiology.techsupport.uk@thermofisher.com
• Phone: +4401256694238
• Email: microbiology.techsupport.uk@thermofisher.com
• Phone: +4401256694238
• Email: microbiology.techsupport.uk@thermofisher.com
• Phone: +4401256694238
• Email: microbiology.techsupport.uk@thermofisher.com
• Phone: +4401256694238
• Email: microbiology.techsupport.uk@thermofisher.com
• Phone: +4401256694238
• Email: microbiology.techsupport.uk@thermofisher.com
• Phone: +4401256694238
• Email: microbiology.techsupport.uk@thermofisher.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05056080501611 [Primary]

FDA Product Code

• GSY: Antisera, Fluorescent, All Globulins, Proteus Spp.

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: 2021-07-29
• Device Publish Date: 2021-07-21

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• 05056080501246 - PathoDx Strep A Grouping Latex: 2021-07-29
• 05056080501253 - PathoDx Strep B Grouping Latex: 2021-07-29
• 05056080501260 - PathoDx Strep C Grouping Latex: 2021-07-29
• 05056080501277 - PathoDx Strep F Grouping Latex: 2021-07-29
• 05056080501284 - PathoDx Strep G Grouping Latex: 2021-07-29