FUKUJU MOXA

GUDID 14979844113005

YAMASHO CO.,LTD.

Moxa

• Primary Device ID: 14979844113005
• NIH Device Record Key: c6abce86-4399-41de-8caf-119d8146a498
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FUKUJU MOXA
• Version Model Number: 10g
• Company DUNS: 703173450
• Company Name: YAMASHO 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	04979844113008 [Primary]
GS1	14979844113005 [Package]; Contains: 04979844113008; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• IMA: Pack, Heat, Moist

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: 2022-12-08
• Device Publish Date: 2022-11-30

On-Brand Devices [FUKUJU MOXA]

• 04979844113053: 200g
• 04979844113046: 100g
• 14979844113005: 10g