mediVR KAGURA

GUDID 14580652420010

MEDIVR, K.K.

Biomechanical function analysis/rehabilitation software

• Primary Device ID: 14580652420010
• NIH Device Record Key: ebab67f9-5e9d-4542-afc9-349cc0cc630e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: mediVR KAGURA
• Version Model Number: MK1
• Company DUNS: 693059749
• Company Name: MEDIVR, K.K.
• 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: false
• Lot Batch: true
• 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	14580652420010 [Primary]

FDA Product Code

• ISD: Exerciser, Measuring

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: 2022-11-18
• Device Publish Date: 2022-11-10