Capio SLIM M0068318250

GUDID 08714729838005

Suture Capturing Device

BOSTON SCIENTIFIC CORPORATION

Suturing unit, single-use

• Primary Device ID: 08714729838005
• NIH Device Record Key: 2d3b33f1-7c8f-4879-86ca-1ee9d3aa3e37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Capio SLIM
• Version Model Number: M0068318250
• Catalog Number: M0068318250
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	08714729838005 [Primary]

FDA Product Code

• PWI: Instrumentation, Surgical Mesh, Urogynecologic, Transvaginal Repair Of Pelvic Organ Prolapse

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2024-11-13
• Device Publish Date: 2016-09-24

On-Brand Devices [Capio SLIM]

• 08714729842224: Suture Capturing Device
• 08714729838005: Suture Capturing Device