Flexible Video-Choledo-Cysto-Ureteroscope

GUDID 06973786290597

Shanghai SeeGen Photoelectric Technology Co., Ltd

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• Primary Device ID: 06973786290597
• NIH Device Record Key: d33294b1-8f33-4ded-8581-9f2fb3e556cc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flexible Video-Choledo-Cysto-Ureteroscope
• Version Model Number: UV-110-E
• Company DUNS: 416472832
• Company Name: Shanghai SeeGen Photoelectric Technology Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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	06973786290597 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211686

FDA Product Code

• FGB: Ureteroscope And Accessories, Flexible/Rigid

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-03
• Device Publish Date: 2023-07-26

On-Brand Devices [Flexible Video-Choledo-Cysto-Ureteroscope]

• 06973786290634: UV-US110-H
• 06973786290627: UV-US100-H
• 06973786290610: UV-110T-E
• 06973786290603: UV-100T-E
• 06973786290597: UV-110-E
• 06973786290580: UV-100-E
• 06973786290573: CHV-US100-H
• 06973786290566: CHV-100T-E
• 06973786290559: CHV-100-E