ScopEYE

GUDID 08800182600041

MediThinQ Co., Ltd.

Endoscopic video image processing unit

• Primary Device ID: 08800182600041
• NIH Device Record Key: fa5f0625-b089-4312-98c6-f4ce2610700e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ScopEYE
• Version Model Number: SE-TXD
• Company DUNS: 695814118
• Company Name: MediThinQ 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: true
• Manufacturing Date: true
• 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	08800182600041 [Primary]

FDA Product Code

• FEM: Accessories, Photographic, For Endoscope (Exclude Light Sources)

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: 2024-02-26
• Device Publish Date: 2024-02-16

On-Brand Devices [ScopEYE]

• 08800182600355: SE-EDNH
• 08800182600331: SE-EDN
• 08800182600195: GV-200 Smart Glasses
• 08800182600041: SE-TXD