Ascend™ Single-Use Flexible Ureteroscope

GUDID 06972520301254

Guangzhou Red Pine Medical Instrument Co., Ltd.

Flexible video ureterorenoscope, single-use

• Primary Device ID: 06972520301254
• NIH Device Record Key: 86cfd71e-632b-4267-9442-7e3a631c8376
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ascend™ Single-Use Flexible Ureteroscope
• Version Model Number: ASUS-86-900R-DC
• 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: Labeling does not contain MRI Safety Information
• 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: 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	06972520301254 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K221158

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: 2026-03-25
• Device Publish Date: 2026-03-17

On-Brand Devices [Ascend™ Single-Use Flexible Ureteroscope]

• 06972520302824: ASUS-75-300S
• 06972520302817: ASUS-75-300R
• 06972520302800: ASUS-75-900S
• 06972520302794: ASUS-75-900R
• 06972520301285: ASUS-86-900S-DC
• 06972520301278: ASUS-86-300S-DC
• 06972520301261: ASUS-86-300R-DC
• 06972520301254: ASUS-86-900R-DC
• 06972520301247: ASUS-86-900S
• 06972520301230: ASUS-86-300S
• 06972520301223: ASUS-86-300R
• 06972520301216: ASUS-86-900R