Disposable Polypectomy Cold Snare

GUDID 06970900855885

Yangzhou Fartley Medical Instrument Technology Co., Ltd

Mechanical-cutting endoscopic polypectomy snare

• Primary Device ID: 06970900855885
• NIH Device Record Key: 39c042ce-2217-47e6-81ae-9ad9e4fe2353
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disposable Polypectomy Cold Snare
• Version Model Number: FTL-PSC-24-230-25-15-R
• Company DUNS: 544375774
• Company Name: Yangzhou Fartley Medical Instrument Technology 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970900855885 [Primary]

FDA Product Code

• FGX: Snare, Non-Electrical

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: 2023-10-27
• Device Publish Date: 2023-10-19

On-Brand Devices [Disposable Polypectomy Cold Snare]

• 06970900855885: FTL-PSC-24-230-25-15-R
• 06970900855878: FTL-PSC-24-230-25-10-R