MicroTest R12533

GUDID 00848838078132

M6 (3.0ml) PK/72

Remel Inc.

Microbiological transport medium IVD

• Primary Device ID: 00848838078132
• NIH Device Record Key: 86cb901b-6bf0-46cd-8258-8e16ba9eb143
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MicroTest
• Version Model Number: R12533
• Catalog Number: R12533
• Company DUNS: 118161628
• Company Name: Remel Inc.
• 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	00848838078132 [Primary]

FDA Product Code

• JSM: Culture Media, Non-Propagating Transport

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: 2023-01-13
• Device Publish Date: 2023-01-05

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• 00848838078132 - MicroTest: 2023-01-13M6 (3.0ml) PK/72
• 00848838078132 - MicroTest: 2023-01-13 M6 (3.0ml) PK/72