Polypectomy Snare

GUDID 16936534300006

NON-ELECTRICAL

Zhejiang Chuangxiang Medical Technology Co., LTD.

Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare Mechanical-cutting endoscopic polypectomy snare

• Primary Device ID: 16936534300006
• NIH Device Record Key: 891de1e2-7cbc-494d-a16c-000c64ebff62
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Polypectomy Snare
• Version Model Number: MD-E-SNC241024
• Company DUNS: 544434963
• Company Name: Zhejiang Chuangxiang Medical 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	06936534300009 [Primary]
GS1	16936534300006 [Package]; Contains: 06936534300009; Package: Box [10 Units]; In Commercial Distribution
GS1	26936534300003 [Package]; Package: Case [5 Units]; In Commercial Distribution

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: 2021-09-03
• Device Publish Date: 2021-08-26

On-Brand Devices [Polypectomy Snare ]

• 16974173020015: NON-ELECTRICAL
• 16974173020008: NON-ELECTRICAL
• 16936534300006: NON-ELECTRICAL