SDJMASTERVISION

GUDID 06974939049000

Tianjin Mastervision Technology Co., Ltd.

Rigid-gas-permeable corrective contact lens, daily-wear

• Primary Device ID: 06974939049000
• NIH Device Record Key: c2eeee88-c4a1-4789-a58f-30c5221f9491
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SDJMASTERVISION
• Version Model Number: MVD01
• Company DUNS: 729799269
• Company Name: Tianjin Mastervision 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: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974939049000 [Primary]

FDA Product Code

• HQD: Lens, Contact (Other Material) - Daily

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: 2025-01-29
• Device Publish Date: 2025-01-21

Devices Manufactured by Tianjin Mastervision Technology Co., Ltd.

• 06974939049000 - SDJMASTERVISION: 2025-01-29
• 06974939049000 - SDJMASTERVISION: 2025-01-29
• 06974939049017 - EyeSpace Bespoke: 2025-01-29 Blue Lens
• 06974939049024 - EyeSpace Bespoke: 2025-01-29 Clear Lens
• 06974939049031 - EyeSpace Scleral: 2025-01-29 Blue Lens
• 06974939049048 - EyeSpace Scleral: 2025-01-29 Clear Lens