Rotatable Snare

GUDID 08714729283997

Single-Use Polypectomy Snare

BOSTON SCIENTIFIC CORPORATION

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

• Primary Device ID: 08714729283997
• NIH Device Record Key: 48497327-8a68-4400-937c-71ac987ec0a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rotatable Snare
• Version Model Number: M00561830
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729283997 [Package]; Contains: 08714729747710; Package: [10 Units]; In Commercial Distribution
GS1	08714729747710 [Primary]

FDA Product Code

• FDI: SNARE, FLEXIBLE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-04-06
• Device Publish Date: 2016-09-24

On-Brand Devices [Rotatable Snare]

• 08714729283997: Single-Use Polypectomy Snare
• 08714729283980: Single-Use Polypectomy Snare