Inami Ophthalmic Instruments

GUDID 04547451333883

Inami Universal Light Weight Trial Frame

INAMI & CO., LTD.

Trial lens frame

• Primary Device ID: 04547451333883
• NIH Device Record Key: a7bdc07c-7668-4363-8efd-b7f475a0e904
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Inami Ophthalmic Instruments
• Version Model Number: K-0391T
• Company DUNS: 690688742
• Company Name: INAMI & 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: true
• 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	04547451333883 [Primary]

FDA Product Code

• HPA: Frame, Trial, Ophthalmic

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: 2025-06-05
• Device Publish Date: 2025-05-28

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• 04547451333883: Inami Universal Light Weight Trial Frame