Single-Use Video Flexible Ureterorenoscope

GUDID 06972520301759

Guangzhou Red Pine Medical Instrument Co., Ltd.

Flexible video ureterorenoscope, single-use

• Primary Device ID: 06972520301759
• NIH Device Record Key: 44268f33-05f0-4b8d-92c3-d45ed20a09f0
• Commercial Distribution Discontinuation: 2025-12-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Single-Use Video Flexible Ureterorenoscope
• Version Model Number: RP-U-C03R9
• Company DUNS: 417649868
• Company Name: Guangzhou Red Pine Medical Instrument 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: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: true
• 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	06972520301759 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K251951

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: 2026-01-08
• Device Publish Date: 2025-12-31

On-Brand Devices [Single-Use Video Flexible Ureterorenoscope]

• 06972520301780: RP-U-C03S3
• 06972520301773: RP-U-C03R3
• 06972520301766: RP-U-C03S9
• 06972520301759: RP-U-C03R9