Capio SLIM

GUDID 08714729842224

Suture Capturing Device

BOSTON SCIENTIFIC CORPORATION

Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use

• Primary Device ID: 08714729842224
• NIH Device Record Key: 5817e0e8-8175-4420-9e26-fa9a5d2bce4e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Capio SLIM
• Version Model Number: M0068318260
• 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	08714729842224 [Package]; Contains: 08714729842804; Package: [5 Units]; In Commercial Distribution
GS1	08714729842804 [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: 6
• Public Version Date: 2020-02-06
• Device Publish Date: 2016-09-24

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• 08714729168782 - Jagwire: 2024-05-15 High Performance Guidewire
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• 08714729168805 - Jagwire: 2024-05-15 High Performance Guidewire