KOOKI

GUDID 04582647306470

MASUNAGA OPTICAL MFG.CO.,LTD.

Spectacle frame

• Primary Device ID: 04582647306470
• NIH Device Record Key: 8b5b1adb-763a-436d-843b-260e28a3a7dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KOOKI
• Version Model Number: KOOKI 573 4 BLACK-SILVER 52
• Company DUNS: 693743585
• Company Name: MASUNAGA OPTICAL MFG.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: false
• 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	04582647306470 [Primary]

FDA Product Code

• HQZ: Frame, Spectacle

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: 2025-06-30
• Device Publish Date: 2025-06-20

On-Brand Devices [KOOKI]

• 04582647306470: KOOKI 573 4 BLACK-SILVER 52
• 04582647306463: KOOKI 573 3 BLUE-GRY 52
• 04582647306456: KOOKI 573 2 D.GRY-BLACK 52
• 04582647306449: KOOKI 573 1 L.BROWN-BLUE 52