STAPHYTECT PLUS

GUDID 05032384029044

OXOID LIMITED

Staphylococcus aureus culture isolate antigen IVD, kit, agglutination

• Primary Device ID: 05032384029044
• NIH Device Record Key: 62ef79fd-0954-4581-9496-5aba32d08873
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STAPHYTECT PLUS
• Version Model Number: DR0850M
• Company DUNS: 365355452
• Company Name: OXOID LIMITED
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05032384029044 [Primary]

FDA Product Code

• JWX: Kit, Screening, Staphylococcus Aureus

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: 2026-02-05
• Device Publish Date: 2026-01-28

On-Brand Devices [STAPHYTECT PLUS]

• 05032384029051: DR0850B
• 05032384029044: DR0850M