MEIDIKE GENE

GUDID 06974931650013

MEDICO TECHNOLOGY CO., LTD

Oral/upper respiratory tract specimen collection swab

• Primary Device ID: 06974931650013
• NIH Device Record Key: dbd00a9e-b011-4ad5-9abf-f1633705b411
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEIDIKE GENE
• Version Model Number: MFS-98000KQ
• Company DUNS: 418826206
• Company Name: MEDICO TECHNOLOGY CO., LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	06974931650013 [Primary]

FDA Product Code

• KXG: Applicator, Absorbent Tipped, Sterile

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-11
• Device Publish Date: 2023-07-03

On-Brand Devices [MEIDIKE GENE]

• 06974931650099: MFS-93000KQ
• 06974931650013: MFS-98000KQ
• 06974931650006: MFS-96000BQ