MicroTest M4RT R12900

GUDID 00842558109718

M4RT(3ml) Dual Swab KIT

Remel Inc.

Microbiological transport medium IVD

• Primary Device ID: 00842558109718
• NIH Device Record Key: 7472ba59-3eba-4054-9b9a-064b3981cb8e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MicroTest M4RT
• Version Model Number: R12900
• Catalog Number: R12900
• 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: 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	00842558109718 [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

On-Brand Devices [MicroTest M4RT]

• 00842558112602: M4RT (3ml) no BEADS Nasal Swab Kit w/bag
• 00842558111209: M4RT(3ml) w/o Beads PK/50
• 00842558110202: M4RT(3ml) 2NPG Swab KIT
• 00842558109718: M4RT(3ml) Dual Swab KIT