UHD series Video Colposcope

GUDID 06944413826731

Edan Instruments, Inc.

Colposcope

• Primary Device ID: 06944413826731
• NIH Device Record Key: 1f091b4e-f79d-4881-8ac8-9514fd5b45c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UHD series Video Colposcope
• Version Model Number: C9 UHD
• Company DUNS: 529173163
• Company Name: Edan Instruments, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06944413826731 [Primary]

FDA Product Code

• PTZ: Colposcope (And Colpomicroscope), Exempt

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: 2025-06-25
• Device Publish Date: 2025-06-17

On-Brand Devices [UHD series Video Colposcope]

• 06944413826809: C12 UHD
• 06944413826731: C9 UHD
• 06944413848559: C12A UHD
• 06944413848542: C9A UHD