EndoVive Standard PEG Kit

GUDID 08714729285199

Percutaneous Endoscopic Gastrostomy Kit

BOSTON SCIENTIFIC CORPORATION

Gastrostomy tube kit, medicated

• Primary Device ID: 08714729285199
• NIH Device Record Key: 4e9285ad-0599-4bce-8f19-23b37bfb4d10
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EndoVive Standard PEG Kit
• Version Model Number: M00568200
• 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: true
• Device Combination Product: true
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729285199 [Package]; Contains: 08714729748687; Package: [2 Units]; In Commercial Distribution
GS1	08714729748687 [Primary]

FDA Product Code

• KNT: TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-10-01
• Device Publish Date: 2016-09-24

On-Brand Devices [EndoVive Standard PEG Kit]

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• 08714729880516: Percutaneous Endoscopic Gastrostomy Kit ENFit
• 08714729880493: Percutaneous Endoscopic Gastrostomy Kit ENFit
• 08714729880479: Percutaneous Endoscopic Gastrostomy Kit ENFit
• 08714729296805: Percutaneous Endoscopic Gastrostomy Kit
• 08714729296799: Percutaneous Endoscopic Gastrostomy Kit
• 08714729285205: Percutaneous Endoscopic Gastrostomy Kit
• 08714729285199: Percutaneous Endoscopic Gastrostomy Kit