PET RPLA KIT

GUDID 05032384028528

OXOID LIMITED

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• Primary Device ID: 05032384028528
• NIH Device Record Key: 4b352e6a-8eb1-4e02-9d35-fc04cf8430b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PET RPLA KIT
• Version Model Number: TD0930A
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05032384028528 [Primary]

FDA Product Code

• JSP: Kit, Anaerobic Identification

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: 2022-12-12
• Device Publish Date: 2022-12-04

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• 05032384011476 - CHLORAMPHENICOL SELECTIVE SUPPLEMENT: 2022-12-15
• 05032384011483 - CHLORAMPHENICOL SELECTIVE SUPPLEMENT: 2022-12-15
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